7-100389718-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389718
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389718
    reference: chr 7
allele count: 2
allele frequency: 1.783962180001784e-5
allele num: 112110
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7659C>G
  hgvsp: ENST00000427578.1:c.7659C>G(p.%3D)
  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.7657C>G
  hgvsp: ENSP00000445943.1:p.Gln2553Glu
  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.7657C>G
  hgvsp: ENSP00000445091.1:p.Gln2553Glu
  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.7657C>G
  hgvsp: ENSP00000444427.1:p.Gln2553Glu
  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.2907C>G
  hgvsp: ENST00000546213.1:c.2907C>G(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.7659C>G
  hgvsp: ENST00000348028.3:c.7659C>G(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.7659C>G
  hgvsp: ENST00000449052.1:c.7659C>G(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.7659C>G
  hgvsp: ENST00000443370.1:c.7659C>G(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.7659C>G
  hgvsp: ENST00000421100.1:c.7659C>G(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.7659C>G
  hgvsp: ENST00000349350.6:c.7659C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14948
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln2553Glu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

7-100389720-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389720
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389720
    reference: chr 7
allele count: 1
allele frequency: 8.955437741796819e-6
allele num: 111664
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.7659G>A
  hgvsp: ENST00000542585.1:c.7659G>A(p.%3D)
  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.7661G>A
  hgvsp: ENSP00000422208.1:p.Arg2554Lys
  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.7661G>A
  hgvsp: ENSP00000422387.1:p.Arg2554Lys
  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.7661G>A
  hgvsp: ENSP00000425200.1:p.Arg2554Lys
  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.7659G>A
  hgvsp: ENST00000546292.1:c.7659G>A(p.%3D)
  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.7661G>A
  hgvsp: ENSP00000423579.1:p.Arg2554Lys
  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.7659G>A
  hgvsp: ENST00000538115.1:c.7659G>A(p.%3D)
  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.7661G>A
  hgvsp: ENSP00000421245.1:p.Arg2554Lys
  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.7661G>A
  hgvsp: ENSP00000425454.1:p.Arg2554Lys
  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.2909G>A
  hgvsp: ENSP00000441117.1:p.Arg970Lys
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5073
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg2554Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

7-100389725-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389725
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389725
    reference: chr 7
allele count: 1
allele frequency: 8.991188635137566e-6
allele num: 111220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7666C>T
  hgvsp: ENSP00000425200.1:p.Pro2556Ser
  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.7666C>T
  hgvsp: ENSP00000422208.1:p.Pro2556Ser
  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.7664C>T
  hgvsp: ENSP00000445943.1:p.Pro2555Leu
  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.7666C>T
  hgvsp: ENSP00000421245.1:p.Pro2556Ser
  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.7666C>T
  hgvsp: ENSP00000422387.1:p.Pro2556Ser
  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.7664C>T
  hgvsp: ENSP00000444427.1:p.Pro2555Leu
  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.2914C>T
  hgvsp: ENSP00000441117.1:p.Pro972Ser
  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.7666C>T
  hgvsp: ENSP00000423579.1:p.Pro2556Ser
  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.7664C>T
  hgvsp: ENSP00000445091.1:p.Pro2555Leu
  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.7666C>T
  hgvsp: ENSP00000425454.1:p.Pro2556Ser
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro2555Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

7-100389726-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389726
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389727
    reference: chr 7
allele count: 1
allele frequency: 8.997012991686761e-6
allele num: 111148
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.7668dupT
  hgvsp: ENSP00000445091.1:p.Ala2557CysfsTer67
  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.7670dupT
  hgvsp: ENSP00000422208.1:p.Leu2557PhefsTer?
  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.7670dupT
  hgvsp: ENSP00000425454.1:p.Leu2557PhefsTer?
  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.7670dupT
  hgvsp: ENSP00000423579.1:p.Leu2557PhefsTer?
  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.7670dupT
  hgvsp: ENSP00000422387.1:p.Leu2557PhefsTer?
  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.7670dupT
  hgvsp: ENSP00000425200.1:p.Leu2557PhefsTer?
  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.7670dupT
  hgvsp: ENSP00000421245.1:p.Leu2557PhefsTer?
  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.2918dupT
  hgvsp: ENSP00000441117.1:p.Leu973PhefsTer69
  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.7668dupT
  hgvsp: ENSP00000445943.1:p.Ala2557CysfsTer72
  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.7668dupT
  hgvsp: ENSP00000444427.1:p.Ala2557CysfsTer278
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ala2557CysfsTer72
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: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

7-100389726-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389726
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389726
    reference: chr 7
allele count: 1
allele frequency: 8.997012991686761e-6
allele num: 111148
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.7667C>T
  hgvsp: ENSP00000421245.1:p.Pro2556Leu
  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.7665C>T
  hgvsp: ENST00000546292.1:c.7665C>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.7665C>T
  hgvsp: ENST00000542585.1:c.7665C>T(p.%3D)
  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.7667C>T
  hgvsp: ENSP00000422387.1:p.Pro2556Leu
  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.7667C>T
  hgvsp: ENSP00000423579.1:p.Pro2556Leu
  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.7667C>T
  hgvsp: ENSP00000422208.1:p.Pro2556Leu
  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.2915C>T
  hgvsp: ENSP00000441117.1:p.Pro972Leu
  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.7665C>T
  hgvsp: ENST00000538115.1:c.7665C>T(p.%3D)
  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.7667C>T
  hgvsp: ENSP00000425454.1:p.Pro2556Leu
  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.7667C>T
  hgvsp: ENSP00000425200.1:p.Pro2556Leu
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro2556Leu
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

7-100389730-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389730
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389730
    reference: chr 7
allele count: 1
allele frequency: 9.021525359507786e-6
allele num: 110846
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.7671G>T
  hgvsp: ENSP00000423579.1:p.Leu2557Phe
  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.7669G>T
  hgvsp: ENSP00000445943.1:p.Ala2557Ser
  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.7671G>T
  hgvsp: ENSP00000425454.1:p.Leu2557Phe
  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.7669G>T
  hgvsp: ENSP00000445091.1:p.Ala2557Ser
  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.7671G>T
  hgvsp: ENSP00000425200.1:p.Leu2557Phe
  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.7671G>T
  hgvsp: ENSP00000421245.1:p.Leu2557Phe
  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.7671G>T
  hgvsp: ENSP00000422387.1:p.Leu2557Phe
  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.7671G>T
  hgvsp: ENSP00000422208.1:p.Leu2557Phe
  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.2919G>T
  hgvsp: ENSP00000441117.1:p.Leu973Phe
  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.7669G>T
  hgvsp: ENSP00000444427.1:p.Ala2557Ser
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala2557Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

7-100389733-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389733
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389733
    reference: chr 7
allele count: 1
allele frequency: 9.06043308870164e-6
allele num: 110370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7674G>A
  hgvsp: ENST00000427578.1:c.7674G>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.7674G>A
  hgvsp: ENST00000449052.1:c.7674G>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.2922G>A
  hgvsp: ENST00000546213.1:c.2922G>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.7674G>A
  hgvsp: ENST00000421100.1:c.7674G>A(p.%3D)
  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.7672G>A
  hgvsp: ENSP00000445091.1:p.Ala2558Thr
  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.7674G>A
  hgvsp: ENST00000349350.6:c.7674G>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.7674G>A
  hgvsp: ENST00000443370.1:c.7674G>A(p.%3D)
  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.7672G>A
  hgvsp: ENSP00000444427.1:p.Ala2558Thr
  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.7672G>A
  hgvsp: ENSP00000445943.1:p.Ala2558Thr
  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.7674G>A
  hgvsp: ENST00000348028.3:c.7674G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala2558Thr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum

7-100389737-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389737
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389737
    reference: chr 7
allele count: 11
allele frequency: 1.006809694662078e-4
allele num: 109256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.7678G>A
  hgvsp: ENSP00000425454.1:p.Val2560Ile
  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.7678G>A
  hgvsp: ENSP00000422208.1:p.Val2560Ile
  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.7676G>A
  hgvsp: ENSP00000445091.1:p.Cys2559Tyr
  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.7678G>A
  hgvsp: ENSP00000423579.1:p.Val2560Ile
  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.2926G>A
  hgvsp: ENSP00000441117.1:p.Val976Ile
  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.7676G>A
  hgvsp: ENSP00000445943.1:p.Cys2559Tyr
  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.7678G>A
  hgvsp: ENSP00000422387.1:p.Val2560Ile
  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.7678G>A
  hgvsp: ENSP00000425200.1:p.Val2560Ile
  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.7678G>A
  hgvsp: ENSP00000421245.1:p.Val2560Ile
  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.7676G>A
  hgvsp: ENSP00000444427.1:p.Cys2559Tyr
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14643
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28323
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6242
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1565
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys2559Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

7-100389742-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389742
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389742
    reference: chr 7
allele count: 19
allele frequency: 1.755358462675536e-4
allele num: 108240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7683C>G
  hgvsp: ENST00000427578.1:c.7683C>G(p.%3D)
  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.7681C>G
  hgvsp: ENSP00000445943.1:p.Gln2561Glu
  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.7683C>G
  hgvsp: ENST00000348028.3:c.7683C>G(p.%3D)
  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.7681C>G
  hgvsp: ENSP00000445091.1:p.Gln2561Glu
  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.7683C>G
  hgvsp: ENST00000449052.1:c.7683C>G(p.%3D)
  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.7681C>G
  hgvsp: ENSP00000444427.1:p.Gln2561Glu
  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.2931C>G
  hgvsp: ENST00000546213.1:c.2931C>G(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.7683C>G
  hgvsp: ENST00000349350.6:c.7683C>G(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.7683C>G
  hgvsp: ENST00000443370.1:c.7683C>G(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.7683C>G
  hgvsp: ENST00000421100.1:c.7683C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27596
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6831
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14317
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln2561Glu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

7-100389742-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389742
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389742
    reference: chr 7
allele count: 1
allele frequency: 9.238728750923873e-6
allele num: 108240
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.7681C>T
  hgvsp: ENSP00000445943.1:p.Gln2561Ter
  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.7683C>T
  hgvsp: ENST00000421100.1:c.7683C>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.7683C>T
  hgvsp: ENST00000349350.6:c.7683C>T(p.%3D)
  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.7681C>T
  hgvsp: ENSP00000444427.1:p.Gln2561Ter
  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.7683C>T
  hgvsp: ENST00000443370.1:c.7683C>T(p.%3D)
  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.7681C>T
  hgvsp: ENSP00000445091.1:p.Gln2561Ter
  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.2931C>T
  hgvsp: ENST00000546213.1:c.2931C>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.7683C>T
  hgvsp: ENST00000427578.1:c.7683C>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.7683C>T
  hgvsp: ENST00000449052.1:c.7683C>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.7683C>T
  hgvsp: ENST00000348028.3:c.7683C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln2561Ter
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

7-100389746-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389746
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389746
    reference: chr 7
allele count: 1
allele frequency: 9.302844809942881e-6
allele num: 107494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7687C>T
  hgvsp: ENSP00000425200.1:p.Arg2563Trp
  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.7687C>T
  hgvsp: ENSP00000423579.1:p.Arg2563Trp
  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.7687C>T
  hgvsp: ENSP00000425454.1:p.Arg2563Trp
  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.7687C>T
  hgvsp: ENSP00000422208.1:p.Arg2563Trp
  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.7685C>T
  hgvsp: ENSP00000444427.1:p.Thr2562Met
  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.7687C>T
  hgvsp: ENSP00000421245.1:p.Arg2563Trp
  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.7685C>T
  hgvsp: ENSP00000445091.1:p.Thr2562Met
  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.7687C>T
  hgvsp: ENSP00000422387.1:p.Arg2563Trp
  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.7685C>T
  hgvsp: ENSP00000445943.1:p.Thr2562Met
  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.2935C>T
  hgvsp: ENSP00000441117.1:p.Arg979Trp
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10500
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr2562Met
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

7-100389748-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389748
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389748
    reference: chr 7
allele count: 1
allele frequency: 9.346842636557371e-6
allele num: 106988
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.7687G>A
  hgvsp: ENSP00000445943.1:p.Val2563Met
  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.7689G>A
  hgvsp: ENST00000449052.1:c.7689G>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.7689G>A
  hgvsp: ENST00000443370.1:c.7689G>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.7689G>A
  hgvsp: ENST00000427578.1:c.7689G>A(p.%3D)
  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.7687G>A
  hgvsp: ENSP00000444427.1:p.Val2563Met
  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.2937G>A
  hgvsp: ENST00000546213.1:c.2937G>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.7689G>A
  hgvsp: ENST00000349350.6:c.7689G>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.7689G>A
  hgvsp: ENST00000348028.3:c.7689G>A(p.%3D)
  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.7687G>A
  hgvsp: ENSP00000445091.1:p.Val2563Met
  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.7689G>A
  hgvsp: ENST00000421100.1:c.7689G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val2563Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

7-100389749-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389749
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389749
    reference: chr 7
allele count: 1
allele frequency: 9.367155007681067e-6
allele num: 106756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7690T>C
  hgvsp: ENSP00000425200.1:p.Trp2564Arg
  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.7688T>C
  hgvsp: ENSP00000445943.1:p.Val2563Ala
  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.7690T>C
  hgvsp: ENSP00000423579.1:p.Trp2564Arg
  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.7688T>C
  hgvsp: ENSP00000444427.1:p.Val2563Ala
  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.7690T>C
  hgvsp: ENSP00000422208.1:p.Trp2564Arg
  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.7690T>C
  hgvsp: ENSP00000421245.1:p.Trp2564Arg
  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.7690T>C
  hgvsp: ENSP00000425454.1:p.Trp2564Arg
  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.7690T>C
  hgvsp: ENSP00000422387.1:p.Trp2564Arg
  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.7688T>C
  hgvsp: ENSP00000445091.1:p.Val2563Ala
  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.2938T>C
  hgvsp: ENSP00000441117.1:p.Trp980Arg
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1824
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val2563Ala
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

7-100389761-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389761
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389761
    reference: chr 7
allele count: 1
allele frequency: 9.629087547663984e-6
allele num: 103852
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.7702C>T
  hgvsp: ENSP00000421245.1:p.Pro2568Ser
  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.7700C>T
  hgvsp: ENSP00000445091.1:p.Pro2567Leu
  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.7700C>T
  hgvsp: ENSP00000444427.1:p.Pro2567Leu
  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.7702C>T
  hgvsp: ENSP00000423579.1:p.Pro2568Ser
  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.7702C>T
  hgvsp: ENSP00000425454.1:p.Pro2568Ser
  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.7702C>T
  hgvsp: ENSP00000422208.1:p.Pro2568Ser
  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.7702C>T
  hgvsp: ENSP00000425200.1:p.Pro2568Ser
  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.7700C>T
  hgvsp: ENSP00000445943.1:p.Pro2567Leu
  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.7702C>T
  hgvsp: ENSP00000422387.1:p.Pro2568Ser
  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.2950C>T
  hgvsp: ENSP00000441117.1:p.Pro984Ser
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24164
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro2567Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum

7-100389764-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389764
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389764
    reference: chr 7
allele count: 1
allele frequency: 9.722330248113867e-6
allele num: 102856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.7705T>C
  hgvsp: ENSP00000421245.1:p.Ser2569Pro
  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.7705T>C
  hgvsp: ENSP00000422387.1:p.Ser2569Pro
  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.7703T>C
  hgvsp: ENSP00000444427.1:p.Phe2568Ser
  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.7705T>C
  hgvsp: ENSP00000425200.1:p.Ser2569Pro
  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.7705T>C
  hgvsp: ENSP00000425454.1:p.Ser2569Pro
  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.7703T>C
  hgvsp: ENSP00000445943.1:p.Phe2568Ser
  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.2953T>C
  hgvsp: ENSP00000441117.1:p.Ser985Pro
  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.7705T>C
  hgvsp: ENSP00000423579.1:p.Ser2569Pro
  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.7705T>C
  hgvsp: ENSP00000422208.1:p.Ser2569Pro
  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.7703T>C
  hgvsp: ENSP00000445091.1:p.Phe2568Ser
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 22962
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11078
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Phe2568Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/7-100389783-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389783
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389783
    reference: chr 7
allele count: 1
allele frequency: 1.044190126138167e-5
allele num: 95768
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.7711+13C>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.7711+13C>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.7709+13C>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.7711+13C>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.7711+13C>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.7709+13C>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.2959+13C>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.7711+13C>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.7711+13C>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.7709+13C>A
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13029
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4359
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1523
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-100389784-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389784
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389784
    reference: chr 7
allele count: 1
allele frequency: 1.047230076447796e-5
allele num: 95490
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.7711+14C>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.7709+14C>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.7709+14C>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.2959+14C>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.7711+14C>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.7711+14C>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.7711+14C>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.7709+14C>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.7711+14C>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.7711+14C>G
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4734
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4503
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22743
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1577
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-100389789-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389789
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389789
    reference: chr 7
allele count: 24
allele frequency: 2.571079639191824e-4
allele num: 93346
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.7709+19A>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.7711+19A>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.7709+19A>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.2959+19A>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.7711+19A>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.7711+19A>C
  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.7709+19A>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.7711+19A>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.7711+19A>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.7711+19A>C
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22827
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9521
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 1.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13488
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

7-100389797-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389797
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389797
    reference: chr 7
allele count: 2
allele frequency: 2.245475367135222e-5
allele num: 89068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.7709+27G>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.7711+27G>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.7711+27G>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.2959+27G>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.7711+27G>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.7711+27G>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.7711+27G>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.7711+27G>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.7709+27G>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.7709+27G>A
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3871
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

7-100389802-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389802
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389801
    reference: chr 7
allele count: 1
allele frequency: 1.16795141322121e-5
allele num: 85620
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.7711+35delC
  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.7711+35delC
  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.2959+35delC
  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.7711+35delC
  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.7709+35delC
  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.7711+35delC
  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.7709+35delC
  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.7709+35delC
  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.7711+35delC
  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.7711+35delC
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5627
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: GC
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

7-100389805-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389805
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389805
    reference: chr 7
allele count: 1
allele frequency: 1.199990400076799e-5
allele num: 83334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.7711+35C>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.7711+35C>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.7709+35C>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.2959+35C>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.7711+35C>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.7709+35C>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.7711+35C>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.7711+35C>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.7711+35C>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.7709+35C>G
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10942
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6037
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4288
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

7-100389809-TGCCTGCTCTGGTCTTTCCCTGGG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389809
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389786
    reference: chr 7
allele count: 1
allele frequency: 1.239095955590801e-5
allele num: 80704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  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
  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
  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
  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
  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
  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
  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
  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
  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
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4634
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19894
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2702
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: TGCCTGCTCTGGTCTTTCCCTGGG
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

7-100389984-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389984
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389983
    reference: chr 7
allele count: 2
allele frequency: 1.785299841108314e-5
allele num: 112026
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.7712-39delC
  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.2960-39delC
  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.7710-39delC
  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.7712-39delC
  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.7712-39delC
  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.7710-39delC
  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.7710-39delC
  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.7712-39delC
  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.7712-39delC
  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.7712-39delC
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3045
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: TC
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

7-100389990-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100389990
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100389990
    reference: chr 7
allele count: 1
allele frequency: 8.905829756158382e-6
allele num: 112286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.7712-37A>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.7712-37A>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.7710-37A>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.7712-37A>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.7710-37A>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.7712-37A>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.7712-37A>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.2960-37A>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.7710-37A>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.7712-37A>G
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2494
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

7-100390012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390012
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390012
    reference: chr 7
allele count: 1
allele frequency: 8.755187448563273e-6
allele num: 114218
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.7712-15C>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.7710-15C>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.2960-15C>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.7712-15C>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.7712-15C>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.7710-15C>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.7710-15C>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.7712-15C>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.7712-15C>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.7712-15C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

7-100390015-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390015
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390015
    reference: chr 7
allele count: 1
allele frequency: 8.728440751344179e-6
allele num: 114568
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.7710-12T>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.7712-12T>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.7712-12T>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.7712-12T>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.7712-12T>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.7710-12T>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.2960-12T>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.7712-12T>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.7712-12T>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.7710-12T>G
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2513
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

7-100390018-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390018
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390017
    reference: chr 7
allele count: 1
allele frequency: 8.706251088281386e-6
allele num: 114860
alternate allele: C
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.7712-8delT
  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.2960-8delT
  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.7710-8delT
  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.7712-8delT
  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.7710-8delT
  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.7712-8delT
  variant of: http://identifiers.org/hgnc/12857
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.7710-8delT
  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.7712-8delT
  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.7712-8delT
  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.7712-8delT
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27525
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 3.25e1
  variant carriers: 0
hgvs: c.7710-8delT
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: CT
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

7-100390021-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390021
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390021
    reference: chr 7
allele count: 5
allele frequency: 4.336438223101074e-5
allele num: 115302
alternate allele: T
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.2960-6C>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.7712-6C>T
  variant of: http://identifiers.org/hgnc/12857
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.7710-6C>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.7710-6C>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.7712-6C>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.7710-6C>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.7712-6C>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.7712-6C>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.7712-6C>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.7712-6C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
hgvs: c.7710-6C>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-100390029-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390029
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390029
    reference: chr 7
allele count: 5
allele frequency: 4.290887870518168e-5
allele num: 116526
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.7712A>C
  hgvsp: ENSP00000445091.1:p.His2571Pro
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.7712A>C
  hgvsp: ENSP00000445943.1:p.His2571Pro
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.7714A>C
  hgvsp: ENSP00000425454.1:p.Thr2572Pro
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.7714A>C
  hgvsp: ENSP00000421245.1:p.Thr2572Pro
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.7714A>C
  hgvsp: ENSP00000423579.1:p.Thr2572Pro
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.2962A>C
  hgvsp: ENSP00000441117.1:p.Thr988Pro
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.7712A>C
  hgvsp: ENSP00000444427.1:p.His2571Pro
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.7714A>C
  hgvsp: ENSP00000422387.1:p.Thr2572Pro
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7714A>C
  hgvsp: ENSP00000425200.1:p.Thr2572Pro
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.7714A>C
  hgvsp: ENSP00000422208.1:p.Thr2572Pro
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.His2571Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

7-100390031-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390031
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390031
    reference: chr 7
allele count: 1
allele frequency: 8.564430208458231e-6
allele num: 116762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.7716T>C
  hgvsp: ENST00000348028.3:c.7716T>C(p.%3D)
  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.7714T>C
  hgvsp: ENSP00000445091.1:p.Cys2572Arg
  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.7716T>C
  hgvsp: ENST00000443370.1:c.7716T>C(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.2964T>C
  hgvsp: ENST00000546213.1:c.2964T>C(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.7716T>C
  hgvsp: ENST00000427578.1:c.7716T>C(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.7716T>C
  hgvsp: ENST00000421100.1:c.7716T>C(p.%3D)
  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.7714T>C
  hgvsp: ENSP00000444427.1:p.Cys2572Arg
  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.7714T>C
  hgvsp: ENSP00000445943.1:p.Cys2572Arg
  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.7716T>C
  hgvsp: ENST00000449052.1:c.7716T>C(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.7716T>C
  hgvsp: ENST00000349350.6:c.7716T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39983
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys2572Arg
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ

7-100390033-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390033
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390033
    reference: chr 7
allele count: 9
allele frequency: 7.696386119140057e-5
allele num: 116938
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.7716C>T
  hgvsp: ENST00000542585.1:c.7716C>T(p.%3D)
  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.7718C>T
  hgvsp: ENSP00000422387.1:p.Ala2573Val
  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.2966C>T
  hgvsp: ENSP00000441117.1:p.Ala989Val
  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.7718C>T
  hgvsp: ENSP00000421245.1:p.Ala2573Val
  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.7718C>T
  hgvsp: ENSP00000422208.1:p.Ala2573Val
  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.7718C>T
  hgvsp: ENSP00000425200.1:p.Ala2573Val
  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.7716C>T
  hgvsp: ENST00000538115.1:c.7716C>T(p.%3D)
  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.7718C>T
  hgvsp: ENSP00000425454.1:p.Ala2573Val
  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.7718C>T
  hgvsp: ENSP00000423579.1:p.Ala2573Val
  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.7716C>T
  hgvsp: ENST00000546292.1:c.7716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala2573Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

7-100390033-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390033
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390033
    reference: chr 7
allele count: 3
allele frequency: 2.565462039713352e-5
allele num: 116938
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.7718C>G
  hgvsp: ENSP00000422208.1:p.Ala2573Gly
  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.7718C>G
  hgvsp: ENSP00000421245.1:p.Ala2573Gly
  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.7718C>G
  hgvsp: ENSP00000425200.1:p.Ala2573Gly
  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.7718C>G
  hgvsp: ENSP00000422387.1:p.Ala2573Gly
  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.7718C>G
  hgvsp: ENSP00000425454.1:p.Ala2573Gly
  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.7716C>G
  hgvsp: ENSP00000445943.1:p.Cys2572Trp
  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.7716C>G
  hgvsp: ENSP00000444427.1:p.Cys2572Trp
  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.7716C>G
  hgvsp: ENSP00000445091.1:p.Cys2572Trp
  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.2966C>G
  hgvsp: ENSP00000441117.1:p.Ala989Gly
  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.7718C>G
  hgvsp: ENSP00000423579.1:p.Ala2573Gly
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Cys2572Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-100390034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390034
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390034
    reference: chr 7
allele count: 13
allele frequency: 1.109328600197973e-4
allele num: 117188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.7719G>A
  hgvsp: ENST00000443370.1:c.7719G>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.7719G>A
  hgvsp: ENST00000348028.3:c.7719G>A(p.%3D)
  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.7717G>A
  hgvsp: ENSP00000444427.1:p.Val2573Met
  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.7717G>A
  hgvsp: ENSP00000445091.1:p.Val2573Met
  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.7719G>A
  hgvsp: ENST00000449052.1:c.7719G>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.2967G>A
  hgvsp: ENST00000546213.1:c.2967G>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.7719G>A
  hgvsp: ENST00000349350.6:c.7719G>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.7719G>A
  hgvsp: ENST00000427578.1:c.7719G>A(p.%3D)
  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.7717G>A
  hgvsp: ENSP00000445943.1:p.Val2573Met
  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.7719G>A
  hgvsp: ENST00000421100.1:c.7719G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val2573Met
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

7-100390045-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390045
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390045
    reference: chr 7
allele count: 2
allele frequency: 1.691503577530066e-5
allele num: 118238
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.7730G>A
  hgvsp: ENSP00000423579.1:p.Cys2577Tyr
  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.7730G>A
  hgvsp: ENSP00000421245.1:p.Cys2577Tyr
  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.7730G>A
  hgvsp: ENSP00000422387.1:p.Cys2577Tyr
  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.7730G>A
  hgvsp: ENSP00000422208.1:p.Cys2577Tyr
  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.7728G>A
  hgvsp: ENST00000546292.1:c.7728G>A(p.%3D)
  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.2978G>A
  hgvsp: ENSP00000441117.1:p.Cys993Tyr
  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.7730G>A
  hgvsp: ENSP00000425454.1:p.Cys2577Tyr
  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.7728G>A
  hgvsp: ENST00000538115.1:c.7728G>A(p.%3D)
  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.7730G>A
  hgvsp: ENSP00000425200.1:p.Cys2577Tyr
  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.7728G>A
  hgvsp: ENST00000542585.1:c.7728G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys2577Tyr
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD

7-100390045-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390045
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390045
    reference: chr 7
allele count: 1
allele frequency: 8.457517887650332e-6
allele num: 118238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.7730G>C
  hgvsp: ENSP00000422387.1:p.Cys2577Ser
  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.7730G>C
  hgvsp: ENSP00000425454.1:p.Cys2577Ser
  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.7730G>C
  hgvsp: ENSP00000422208.1:p.Cys2577Ser
  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.7730G>C
  hgvsp: ENSP00000421245.1:p.Cys2577Ser
  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.7728G>C
  hgvsp: ENST00000538115.1:c.7728G>C(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.7728G>C
  hgvsp: ENST00000546292.1:c.7728G>C(p.%3D)
  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.2978G>C
  hgvsp: ENSP00000441117.1:p.Cys993Ser
  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.7730G>C
  hgvsp: ENSP00000423579.1:p.Cys2577Ser
  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.7730G>C
  hgvsp: ENSP00000425200.1:p.Cys2577Ser
  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.7728G>C
  hgvsp: ENST00000542585.1:c.7728G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1356
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Cys2577Ser
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS

7-100390055-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390055
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390055
    reference: chr 7
allele count: 1
allele frequency: 8.420485356775965e-6
allele num: 118758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.7738C>T
  hgvsp: ENSP00000444427.1:p.Gln2580Ter
  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.7738C>T
  hgvsp: ENSP00000445091.1:p.Gln2580Ter
  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.7738C>T
  hgvsp: ENSP00000445943.1:p.Gln2580Ter
  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.7740C>T
  hgvsp: ENST00000443370.1:c.7740C>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.2988C>T
  hgvsp: ENST00000546213.1:c.2988C>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.7740C>T
  hgvsp: ENST00000421100.1:c.7740C>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.7740C>T
  hgvsp: ENST00000427578.1:c.7740C>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.7740C>T
  hgvsp: ENST00000449052.1:c.7740C>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.7740C>T
  hgvsp: ENST00000349350.6:c.7740C>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.7740C>T
  hgvsp: ENST00000348028.3:c.7740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln2580Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

7-100390057-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390057
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390057
    reference: chr 7
allele count: 1
allele frequency: 8.414391976035812e-6
allele num: 118844
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.7740G>T
  hgvsp: ENSP00000444427.1:p.Gln2580His
  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.7742G>T
  hgvsp: ENSP00000421245.1:p.Arg2581Met
  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.7742G>T
  hgvsp: ENSP00000425454.1:p.Arg2581Met
  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.7742G>T
  hgvsp: ENSP00000423579.1:p.Arg2581Met
  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.7742G>T
  hgvsp: ENSP00000422387.1:p.Arg2581Met
  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.7740G>T
  hgvsp: ENSP00000445091.1:p.Gln2580His
  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.7742G>T
  hgvsp: ENSP00000425200.1:p.Arg2581Met
  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.7740G>T
  hgvsp: ENSP00000445943.1:p.Gln2580His
  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.7742G>T
  hgvsp: ENSP00000422208.1:p.Arg2581Met
  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.2990G>T
  hgvsp: ENSP00000441117.1:p.Arg997Met
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln2580His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

7-100390063-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390063
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390063
    reference: chr 7
allele count: 2
allele frequency: 1.681576646263537e-5
allele num: 118936
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.7748A>G
  hgvsp: ENSP00000425454.1:p.Gln2583Arg
  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.7748A>G
  hgvsp: ENSP00000425200.1:p.Gln2583Arg
  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.7746A>G
  hgvsp: ENST00000538115.1:c.7746A>G(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.7746A>G
  hgvsp: ENST00000542585.1:c.7746A>G(p.%3D)
  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.7748A>G
  hgvsp: ENSP00000423579.1:p.Gln2583Arg
  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.7748A>G
  hgvsp: ENSP00000422387.1:p.Gln2583Arg
  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.7748A>G
  hgvsp: ENSP00000421245.1:p.Gln2583Arg
  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.7748A>G
  hgvsp: ENSP00000422208.1:p.Gln2583Arg
  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.7746A>G
  hgvsp: ENST00000546292.1:c.7746A>G(p.%3D)
  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.2996A>G
  hgvsp: ENSP00000441117.1:p.Gln999Arg
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln2583Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

7-100390064-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390064
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390064
    reference: chr 7
allele count: 2
allele frequency: 1.681633202165944e-5
allele num: 118932
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.7747A>G
  hgvsp: ENSP00000445091.1:p.Arg2583Gly
  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.7749A>G
  hgvsp: ENST00000427578.1:c.7749A>G(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.7749A>G
  hgvsp: ENST00000349350.6:c.7749A>G(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.7749A>G
  hgvsp: ENST00000443370.1:c.7749A>G(p.%3D)
  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.7747A>G
  hgvsp: ENSP00000444427.1:p.Arg2583Gly
  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.7749A>G
  hgvsp: ENST00000348028.3:c.7749A>G(p.%3D)
  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.7747A>G
  hgvsp: ENSP00000445943.1:p.Arg2583Gly
  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.7749A>G
  hgvsp: ENST00000421100.1:c.7749A>G(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.2997A>G
  hgvsp: ENST00000546213.1:c.2997A>G(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.7749A>G
  hgvsp: ENST00000449052.1:c.7749A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg2583Gly
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: A
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

7-100390075-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390075
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390075
    reference: chr 7
allele count: 2
allele frequency: 1.681152598221341e-5
allele num: 118966
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.7760G>A
  hgvsp: ENSP00000423579.1:p.Arg2587Lys
  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.7760G>A
  hgvsp: ENSP00000422387.1:p.Arg2587Lys
  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.7758G>A
  hgvsp: ENST00000546292.1:c.7758G>A(p.%3D)
  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.7760G>A
  hgvsp: ENSP00000425200.1:p.Arg2587Lys
  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.3008G>A
  hgvsp: ENSP00000441117.1:p.Arg1003Lys
  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.7760G>A
  hgvsp: ENSP00000425454.1:p.Arg2587Lys
  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.7758G>A
  hgvsp: ENST00000538115.1:c.7758G>A(p.%3D)
  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.7760G>A
  hgvsp: ENSP00000421245.1:p.Arg2587Lys
  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.7760G>A
  hgvsp: ENSP00000422208.1:p.Arg2587Lys
  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.7758G>A
  hgvsp: ENST00000542585.1:c.7758G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg2587Lys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

7-100390078-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390078
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390078
    reference: chr 7
allele count: 1
allele frequency: 8.406752303450132e-6
allele num: 118952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7763G>A
  hgvsp: ENSP00000425200.1:p.Ser2588Asn
  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.7761G>A
  hgvsp: ENST00000546292.1:c.7761G>A(p.%3D)
  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.7763G>A
  hgvsp: ENSP00000423579.1:p.Ser2588Asn
  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.7761G>A
  hgvsp: ENST00000538115.1:c.7761G>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.7761G>A
  hgvsp: ENST00000542585.1:c.7761G>A(p.%3D)
  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.7763G>A
  hgvsp: ENSP00000421245.1:p.Ser2588Asn
  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.3011G>A
  hgvsp: ENSP00000441117.1:p.Ser1004Asn
  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.7763G>A
  hgvsp: ENSP00000425454.1:p.Ser2588Asn
  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.7763G>A
  hgvsp: ENSP00000422387.1:p.Ser2588Asn
  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.7763G>A
  hgvsp: ENSP00000422208.1:p.Ser2588Asn
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser2588Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

7-100390082-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390082
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390082
    reference: chr 7
allele count: 20
allele frequency: 1.681661481543765e-4
allele num: 118930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.7767C>T
  hgvsp: ENST00000421100.1:c.7767C>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.7767C>T
  hgvsp: ENST00000349350.6:c.7767C>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.7767C>T
  hgvsp: ENST00000443370.1:c.7767C>T(p.%3D)
  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.7765C>T
  hgvsp: ENSP00000445091.1:p.Arg2589Cys
  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.7767C>T
  hgvsp: ENST00000449052.1:c.7767C>T(p.%3D)
  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.7765C>T
  hgvsp: ENSP00000444427.1:p.Arg2589Cys
  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.7767C>T
  hgvsp: ENST00000348028.3:c.7767C>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.7767C>T
  hgvsp: ENST00000427578.1:c.7767C>T(p.%3D)
  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.7765C>T
  hgvsp: ENSP00000445943.1:p.Arg2589Cys
  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.3015C>T
  hgvsp: ENST00000546213.1:c.3015C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10598
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28686
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15935
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg2589Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

7-100390083-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390083
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390083
    reference: chr 7
allele count: 3
allele frequency: 2.522492222315648e-5
allele num: 118930
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.7766G>A
  hgvsp: ENSP00000445943.1:p.Arg2589His
  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.7768G>A
  hgvsp: ENSP00000425200.1:p.Val2590Ile
  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.7768G>A
  hgvsp: ENSP00000425454.1:p.Val2590Ile
  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.7768G>A
  hgvsp: ENSP00000421245.1:p.Val2590Ile
  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.7766G>A
  hgvsp: ENSP00000444427.1:p.Arg2589His
  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.7768G>A
  hgvsp: ENSP00000423579.1:p.Val2590Ile
  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.7766G>A
  hgvsp: ENSP00000445091.1:p.Arg2589His
  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.7768G>A
  hgvsp: ENSP00000422208.1:p.Val2590Ile
  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.7768G>A
  hgvsp: ENSP00000422387.1:p.Val2590Ile
  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.3016G>A
  hgvsp: ENSP00000441117.1:p.Val1006Ile
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28703
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg2589His
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

7-100390084-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390084
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390084
    reference: chr 7
allele count: 2
allele frequency: 1.681718043152885e-5
allele num: 118926
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.7769T>C
  hgvsp: ENSP00000421245.1:p.Val2590Ala
  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.7767T>C
  hgvsp: ENST00000538115.1:c.7767T>C(p.%3D)
  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.7769T>C
  hgvsp: ENSP00000425454.1:p.Val2590Ala
  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.7769T>C
  hgvsp: ENSP00000425200.1:p.Val2590Ala
  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.7769T>C
  hgvsp: ENSP00000423579.1:p.Val2590Ala
  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.7767T>C
  hgvsp: ENST00000542585.1:c.7767T>C(p.%3D)
  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.7769T>C
  hgvsp: ENSP00000422208.1:p.Val2590Ala
  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.7769T>C
  hgvsp: ENSP00000422387.1:p.Val2590Ala
  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.7767T>C
  hgvsp: ENST00000546292.1:c.7767T>C(p.%3D)
  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.3017T>C
  hgvsp: ENSP00000441117.1:p.Val1006Ala
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val2590Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

7-100390091-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390091
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390091
    reference: chr 7
allele count: 5
allele frequency: 4.210384492311838e-5
allele num: 118754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.7776G>A
  hgvsp: ENST00000443370.1:c.7776G>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.7776G>A
  hgvsp: ENST00000427578.1:c.7776G>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.3024G>A
  hgvsp: ENST00000546213.1:c.3024G>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.7776G>A
  hgvsp: ENST00000349350.6:c.7776G>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.7776G>A
  hgvsp: ENST00000449052.1:c.7776G>A(p.%3D)
  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.7774G>A
  hgvsp: ENSP00000445943.1:p.Val2592Ile
  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.7774G>A
  hgvsp: ENSP00000445091.1:p.Val2592Ile
  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.7774G>A
  hgvsp: ENSP00000444427.1:p.Val2592Ile
  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.7776G>A
  hgvsp: ENST00000348028.3:c.7776G>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.7776G>A
  hgvsp: ENST00000421100.1:c.7776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val2592Ile
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-100390093-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390093
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390093
    reference: chr 7
allele count: 1
allele frequency: 8.422613031466883e-6
allele num: 118728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.7778C>A
  hgvsp: ENSP00000425454.1:p.Ser2593Tyr
  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.7776C>A
  hgvsp: ENST00000542585.1:c.7776C>A(p.%3D)
  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.7778C>A
  hgvsp: ENSP00000423579.1:p.Ser2593Tyr
  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.7776C>A
  hgvsp: ENST00000546292.1:c.7776C>A(p.%3D)
  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.3026C>A
  hgvsp: ENSP00000441117.1:p.Ser1009Tyr
  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.7778C>A
  hgvsp: ENSP00000422208.1:p.Ser2593Tyr
  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.7778C>A
  hgvsp: ENSP00000421245.1:p.Ser2593Tyr
  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.7778C>A
  hgvsp: ENSP00000422387.1:p.Ser2593Tyr
  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.7778C>A
  hgvsp: ENSP00000425200.1:p.Ser2593Tyr
  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.7776C>A
  hgvsp: ENST00000538115.1:c.7776C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser2593Tyr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

7-100390105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390105
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390105
    reference: chr 7
allele count: 3
allele frequency: 2.537427048972342e-5
allele num: 118230
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.7790C>T
  hgvsp: ENSP00000421245.1:p.Thr2597Met
  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.3038C>T
  hgvsp: ENSP00000441117.1:p.Thr1013Met
  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.7786+4C>T
  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.7788C>T
  hgvsp: ENST00000546292.1:c.7788C>T(p.%3D)
  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.7790C>T
  hgvsp: ENSP00000425200.1:p.Thr2597Met
  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.7790C>T
  hgvsp: ENSP00000423579.1:p.Thr2597Met
  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.7788C>T
  hgvsp: ENST00000542585.1:c.7788C>T(p.%3D)
  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.7786+4C>T
  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.7788C>T
  hgvsp: ENST00000538115.1:c.7788C>T(p.%3D)
  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.7790C>T
  hgvsp: ENSP00000422208.1:p.Thr2597Met
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1759
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr1013Met
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP

7-100390109-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390109
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390109
    reference: chr 7
allele count: 2
allele frequency: 1.693766937669377e-5
allele num: 118080
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.7792A>G
  hgvsp: ENSP00000445943.1:p.Ile2598Val
  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.7786+8A>G
  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.7794A>G
  hgvsp: ENST00000449052.1:c.7794A>G(p.%3D)
  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.7786+8A>G
  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.7792A>G
  hgvsp: ENSP00000445091.1:p.Ile2598Val
  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.7794A>G
  hgvsp: ENST00000443370.1:c.7794A>G(p.%3D)
  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.7792A>G
  hgvsp: ENSP00000444427.1:p.Ile2598Val
  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.7794A>G
  hgvsp: ENST00000427578.1:c.7794A>G(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.3042A>G
  hgvsp: ENST00000546213.1:c.3042A>G(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.7794A>G
  hgvsp: ENST00000348028.3:c.7794A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile2598Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-100390122-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390122
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390122
    reference: chr 7
allele count: 1
allele frequency: 8.571771442286263e-6
allele num: 116662
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.7807A>G
  hgvsp: ENSP00000421245.1:p.Arg2603Gly
  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.7805A>G
  hgvsp: ENSP00000445091.1:p.Glu2602Gly
  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.7807A>G
  hgvsp: ENSP00000422208.1:p.Arg2603Gly
  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.7807A>G
  hgvsp: ENSP00000423579.1:p.Arg2603Gly
  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.7805A>G
  hgvsp: ENSP00000445943.1:p.Glu2602Gly
  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.7786+21A>G
  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.7805A>G
  hgvsp: ENSP00000444427.1:p.Glu2602Gly
  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.7786+21A>G
  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.3055A>G
  hgvsp: ENSP00000441117.1:p.Arg1019Gly
  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.7807A>G
  hgvsp: ENSP00000425200.1:p.Arg2603Gly
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu2602Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

7-100390125-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390125
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390125
    reference: chr 7
allele count: 7
allele frequency: 6.02471855957586e-5
allele num: 116188
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.3058C>G
  hgvsp: ENSP00000441117.1:p.Arg1020Gly
  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.7808C>G
  hgvsp: ENSP00000445091.1:p.Ala2603Gly
  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.7808C>G
  hgvsp: ENSP00000445943.1:p.Ala2603Gly
  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.7810C>G
  hgvsp: ENSP00000422208.1:p.Arg2604Gly
  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.7786+24C>G
  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.7810C>G
  hgvsp: ENSP00000421245.1:p.Arg2604Gly
  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.7810C>G
  hgvsp: ENSP00000425200.1:p.Arg2604Gly
  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.7808C>G
  hgvsp: ENSP00000444427.1:p.Ala2603Gly
  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.7786+24C>G
  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.7810C>G
  hgvsp: ENSP00000423579.1:p.Arg2604Gly
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9052
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2144
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala2603Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-100390126-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390126
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390126
    reference: chr 7
allele count: 4
allele frequency: 3.444178477328695e-5
allele num: 116138
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.3059G>A
  hgvsp: ENSP00000441117.1:p.Arg1020Gln
  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.7811G>A
  hgvsp: ENSP00000422208.1:p.Arg2604Gln
  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.7809G>A
  hgvsp: ENST00000538115.1:c.7809G>A(p.%3D)
  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.7786+25G>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.7786+25G>A
  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.7811G>A
  hgvsp: ENSP00000423579.1:p.Arg2604Gln
  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.7811G>A
  hgvsp: ENSP00000421245.1:p.Arg2604Gln
  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.7811G>A
  hgvsp: ENSP00000425200.1:p.Arg2604Gln
  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.7809G>A
  hgvsp: ENST00000546292.1:c.7809G>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.7809G>A
  hgvsp: ENST00000542585.1:c.7809G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8930
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg1020Gln
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

7-100390129-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390129
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390129
    reference: chr 7
allele count: 2
allele frequency: 1.72824997407625e-5
allele num: 115724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7814C>T
  hgvsp: ENSP00000425200.1:p.Ala2605Val
  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.3062C>T
  hgvsp: ENSP00000441117.1:p.Ala1021Val
  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.7812C>T
  hgvsp: ENST00000538115.1:c.7812C>T(p.%3D)
  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.7814C>T
  hgvsp: ENSP00000421245.1:p.Ala2605Val
  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.7812C>T
  hgvsp: ENST00000542585.1:c.7812C>T(p.%3D)
  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.7786+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.7786+28C>T
  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.7814C>T
  hgvsp: ENSP00000422208.1:p.Ala2605Val
  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.7812C>T
  hgvsp: ENST00000546292.1:c.7812C>T(p.%3D)
  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.7814C>T
  hgvsp: ENSP00000423579.1:p.Ala2605Val
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8625
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala1021Val
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

7-100390130-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390130
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390130
    reference: chr 7
allele count: 1
allele frequency: 8.689456213830139e-6
allele num: 115082
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.7786+29G>A
  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.7815G>A
  hgvsp: ENST00000348028.3:c.7815G>A(p.%3D)
  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.7813G>A
  hgvsp: ENSP00000445943.1:p.Ala2605Thr
  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.7815G>A
  hgvsp: ENST00000443370.1:c.7815G>A(p.%3D)
  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.7813G>A
  hgvsp: ENSP00000445091.1:p.Ala2605Thr
  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.7815G>A
  hgvsp: ENST00000427578.1:c.7815G>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.3063G>A
  hgvsp: ENST00000546213.1:c.3063G>A(p.%3D)
  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.7813G>A
  hgvsp: ENSP00000444427.1:p.Ala2605Thr
  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.7815G>A
  hgvsp: ENST00000449052.1:c.7815G>A(p.%3D)
  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.7786+29G>A
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8424
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7573
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala2605Thr
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

7-100390135-C-CCTGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390135
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390139
    reference: chr 7
allele count: 20
allele frequency: 1.741583796304359e-4
allele num: 114838
alternate allele: CCTGG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7830_7833dupTGGC
  hgvsp: ENSP00000425200.1:p.Gly2612TrpfsTer?
  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.3078_3081dupTGGC
  hgvsp: ENSP00000441117.1:p.Gly1028TrpfsTer15
  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.7828_7831dupTGGC
  hgvsp: ENSP00000445943.1:p.Arg2611LeufsTer19
  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.7786+44_7786+47dupTGGC
  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.7830_7833dupTGGC
  hgvsp: ENSP00000421245.1:p.Gly2612TrpfsTer?
  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.7828_7831dupTGGC
  hgvsp: ENSP00000445091.1:p.Arg2611LeufsTer14
  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.7828_7831dupTGGC
  hgvsp: ENSP00000444427.1:p.Arg2611LeufsTer225
  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.7786+44_7786+47dupTGGC
  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.7830_7833dupTGGC
  hgvsp: ENSP00000422208.1:p.Gly2612TrpfsTer?
  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.7830_7833dupTGGC
  hgvsp: ENSP00000423579.1:p.Gly2612TrpfsTer?
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15106
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26098
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2058
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg2611LeufsTer19
num of homozygotes: 1
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

7-100390137-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390137
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390137
    reference: chr 7
allele count: 1
allele frequency: 8.805917576611483e-6
allele num: 113560
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.7822T>G
  hgvsp: ENSP00000421245.1:p.Trp2608Gly
  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.7820T>G
  hgvsp: ENSP00000445943.1:p.Leu2607Arg
  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.7822T>G
  hgvsp: ENSP00000425200.1:p.Trp2608Gly
  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.3070T>G
  hgvsp: ENSP00000441117.1:p.Trp1024Gly
  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.7786+36T>G
  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.7820T>G
  hgvsp: ENSP00000445091.1:p.Leu2607Arg
  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.7820T>G
  hgvsp: ENSP00000444427.1:p.Leu2607Arg
  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.7786+36T>G
  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.7822T>G
  hgvsp: ENSP00000422208.1:p.Trp2608Gly
  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.7822T>G
  hgvsp: ENSP00000423579.1:p.Trp2608Gly
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6661
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu2607Arg
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

7-100390146-GGC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390146
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390144
    reference: chr 7
allele count: 1
allele frequency: 8.967323074715735e-6
allele num: 111516
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.7833_7834delCG
  hgvsp: ENSP00000423579.1:p.Gly2612AspfsTer?
  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.7833_7834delCG
  hgvsp: ENSP00000422208.1:p.Gly2612AspfsTer?
  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.7831_7832delCG
  hgvsp: ENSP00000445943.1:p.Arg2611GlyfsTer17
  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.7786+47_7786+48delCG
  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.7833_7834delCG
  hgvsp: ENSP00000421245.1:p.Gly2612AspfsTer?
  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.3081_3082delCG
  hgvsp: ENSP00000441117.1:p.Gly1028AspfsTer13
  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.7831_7832delCG
  hgvsp: ENSP00000444427.1:p.Arg2611GlyfsTer223
  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.7786+47_7786+48delCG
  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.7833_7834delCG
  hgvsp: ENSP00000425200.1:p.Gly2612AspfsTer?
  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.7831_7832delCG
  hgvsp: ENSP00000445091.1:p.Arg2611GlyfsTer12
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14892
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1975
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg2611GlyfsTer17
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: GGC
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

7-100390149-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390149
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390149
    reference: chr 7
allele count: 1683
allele frequency: 1.520902239331996e-2
allele num: 110658
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.7786+48G>A
  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.3082G>A
  hgvsp: ENSP00000441117.1:p.Gly1028Arg
  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.7834G>A
  hgvsp: ENSP00000421245.1:p.Gly2612Arg
  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.7834G>A
  hgvsp: ENSP00000422208.1:p.Gly2612Arg
  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.7834G>A
  hgvsp: ENSP00000423579.1:p.Gly2612Arg
  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.7832G>A
  hgvsp: ENSP00000445091.1:p.Arg2611Gln
  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.7832G>A
  hgvsp: ENSP00000444427.1:p.Arg2611Gln
  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.7834G>A
  hgvsp: ENSP00000425200.1:p.Gly2612Arg
  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.7832G>A
  hgvsp: ENSP00000445943.1:p.Arg2611Gln
  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.7786+48G>A
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5661
  bin: 3.25e1
  variant carriers: 304
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 1.75e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 1.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 176
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.75e1
  variant carriers: 239
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21876
  bin: 2.75e1
  variant carriers: 271
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 7.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 15456
  bin: 2.25e1
  variant carriers: 247
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1511
  bin: 7.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg2611Gln
num of homozygotes: 20
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

7-100390151-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390151
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390152
    reference: chr 7
allele count: 1
allele frequency: 9.070788432930591e-6
allele num: 110244
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.7835dupA
  hgvsp: ENSP00000445091.1:p.Asp2612GlufsTer12
  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.7837dupA
  hgvsp: ENSP00000422208.1:p.Thr2613AsnfsTer?
  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.7837dupA
  hgvsp: ENSP00000421245.1:p.Thr2613AsnfsTer?
  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.7786+51dupA
  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.7835dupA
  hgvsp: ENSP00000445943.1:p.Asp2612GlufsTer17
  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.7837dupA
  hgvsp: ENSP00000423579.1:p.Thr2613AsnfsTer?
  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.7837dupA
  hgvsp: ENSP00000425200.1:p.Thr2613AsnfsTer?
  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.7835dupA
  hgvsp: ENSP00000444427.1:p.Asp2612GlufsTer223
  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.7786+51dupA
  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.3085dupA
  hgvsp: ENSP00000441117.1:p.Thr1029AsnfsTer13
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 21795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5672
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp2612GlufsTer17
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

7-100390154-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390154
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390154
    reference: chr 7
allele count: 4
allele frequency: 3.668445862910178e-5
allele num: 109038
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.7837C>T
  hgvsp: ENSP00000445091.1:p.Arg2613Cys
  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.7839C>T
  hgvsp: ENST00000348028.3:c.7839C>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.3087C>T
  hgvsp: ENST00000546213.1:c.3087C>T(p.%3D)
  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.7786+53C>T
  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.7839C>T
  hgvsp: ENST00000449052.1:c.7839C>T(p.%3D)
  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.7786+53C>T
  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.7839C>T
  hgvsp: ENST00000443370.1:c.7839C>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.7839C>T
  hgvsp: ENST00000427578.1:c.7839C>T(p.%3D)
  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.7837C>T
  hgvsp: ENSP00000444427.1:p.Arg2613Cys
  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.7837C>T
  hgvsp: ENSP00000445943.1:p.Arg2613Cys
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15215
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg2613Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

7-100390155-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390155
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390155
    reference: chr 7
allele count: 9
allele frequency: 8.340747330960854e-5
allele num: 107904
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.7838G>A
  hgvsp: ENSP00000444427.1:p.Arg2613His
  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.7840G>A
  hgvsp: ENSP00000423579.1:p.Ala2614Thr
  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.7840G>A
  hgvsp: ENSP00000425200.1:p.Ala2614Thr
  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.3088G>A
  hgvsp: ENSP00000441117.1:p.Ala1030Thr
  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.7840G>A
  hgvsp: ENSP00000421245.1:p.Ala2614Thr
  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.7786+54G>A
  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.7840G>A
  hgvsp: ENSP00000422208.1:p.Ala2614Thr
  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.7838G>A
  hgvsp: ENSP00000445091.1:p.Arg2613His
  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.7786+54G>A
  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.7838G>A
  hgvsp: ENSP00000445943.1:p.Arg2613His
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15034
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19505
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27688
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg2613His
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

7-100390156-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390156
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390156
    reference: chr 7
allele count: 1
allele frequency: 9.249495902473315e-6
allele num: 108114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.7841C>T
  hgvsp: ENSP00000423579.1:p.Ala2614Val
  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.7786+55C>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.7786+55C>T
  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.7841C>T
  hgvsp: ENSP00000425200.1:p.Ala2614Val
  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.7839C>T
  hgvsp: ENST00000546292.1:c.7839C>T(p.%3D)
  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.7841C>T
  hgvsp: ENSP00000421245.1:p.Ala2614Val
  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.7839C>T
  hgvsp: ENST00000538115.1:c.7839C>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.7839C>T
  hgvsp: ENST00000542585.1:c.7839C>T(p.%3D)
  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.7841C>T
  hgvsp: ENSP00000422208.1:p.Ala2614Val
  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.3089C>T
  hgvsp: ENSP00000441117.1:p.Ala1030Val
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5010
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala1030Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

7-100390161-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390161
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390161
    reference: chr 7
allele count: 3
allele frequency: 2.806098587597044e-5
allele num: 106910
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.7844T>C
  hgvsp: ENSP00000445091.1:p.Leu2615Pro
  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.7846T>C
  hgvsp: ENSP00000423579.1:p.Ser2616Pro
  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.7844T>C
  hgvsp: ENSP00000444427.1:p.Leu2615Pro
  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.7846T>C
  hgvsp: ENSP00000422208.1:p.Ser2616Pro
  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.7846T>C
  hgvsp: ENSP00000421245.1:p.Ser2616Pro
  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.7844T>C
  hgvsp: ENSP00000445943.1:p.Leu2615Pro
  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.3094T>C
  hgvsp: ENSP00000441117.1:p.Ser1032Pro
  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.7786+60T>C
  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.7846T>C
  hgvsp: ENSP00000425200.1:p.Ser2616Pro
  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.7786+60T>C
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15188
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu2615Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-100390162-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390162
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390162
    reference: chr 7
allele count: 3
allele frequency: 2.812095761234322e-5
allele num: 106682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7847C>A
  hgvsp: ENSP00000425200.1:p.Ser2616Tyr
  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.7847C>A
  hgvsp: ENSP00000423579.1:p.Ser2616Tyr
  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.7786+61C>A
  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.7847C>A
  hgvsp: ENSP00000421245.1:p.Ser2616Tyr
  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.7845C>A
  hgvsp: ENST00000546292.1:c.7845C>A(p.%3D)
  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.3095C>A
  hgvsp: ENSP00000441117.1:p.Ser1032Tyr
  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.7786+61C>A
  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.7845C>A
  hgvsp: ENST00000538115.1:c.7845C>A(p.%3D)
  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.7847C>A
  hgvsp: ENSP00000422208.1:p.Ser2616Tyr
  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.7845C>A
  hgvsp: ENST00000542585.1:c.7845C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17547
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser1032Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP

7-100390165-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390165
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390165
    reference: chr 7
allele count: 174
allele frequency: 1.649414173586623e-3
allele num: 105492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.7850C>T
  hgvsp: ENSP00000421245.1:p.Ala2617Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7850C>T
  hgvsp: ENSP00000425200.1:p.Ala2617Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.7848C>T
  hgvsp: ENST00000542585.1:c.7848C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.7850C>T
  hgvsp: ENSP00000422208.1:p.Ala2617Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.3098C>T
  hgvsp: ENSP00000441117.1:p.Ala1033Val
  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.7786+64C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.7848C>T
  hgvsp: ENST00000538115.1:c.7848C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.7848C>T
  hgvsp: ENST00000546292.1:c.7848C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.7850C>T
  hgvsp: ENSP00000423579.1:p.Ala2617Val
  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.7786+64C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 1.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15435
  bin: 2.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12201
  bin: 1.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16241
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: p.Ala1033Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP

7-100390166-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390166
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390166
    reference: chr 7
allele count: 70
allele frequency: 6.647673314339981e-4
allele num: 105300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.3099G>A
  hgvsp: ENST00000546213.1:c.3099G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.7849G>A
  hgvsp: ENSP00000445091.1:p.Ala2617Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.7851G>A
  hgvsp: ENST00000348028.3:c.7851G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.7851G>A
  hgvsp: ENST00000449052.1:c.7851G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7851G>A
  hgvsp: ENST00000427578.1:c.7851G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.7849G>A
  hgvsp: ENSP00000444427.1:p.Ala2617Thr
  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.7786+65G>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.7786+65G>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.7849G>A
  hgvsp: ENSP00000445943.1:p.Glu2617Lys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.7851G>A
  hgvsp: ENST00000443370.1:c.7851G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15568
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15986
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 6550
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12479
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu2617Lys
num of homozygotes: 1
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD

7-100390170-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390170
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390170
    reference: chr 7
allele count: 1
allele frequency: 9.562423500611994e-6
allele num: 104576
alternate allele: G
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.7851+4A>G
  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.3099+4A>G
  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.7849+4A>G
  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.7851+4A>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.7786+69A>G
  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.7851+4A>G
  variant of: http://identifiers.org/hgnc/12857
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.7849+4A>G
  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.7851+4A>G
  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.7849+4A>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.7786+69A>G
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14898
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3450
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 4.25e1
  variant carriers: 0
hgvs: c.7849+4A>G
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum

7-100390171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390171
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390171
    reference: chr 7
allele count: 1
allele frequency: 9.582399049426015e-6
allele num: 104358
alternate allele: A
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.7849+5G>A
  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.7851+5G>A
  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.7851+5G>A
  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.3099+5G>A
  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.7849+5G>A
  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.7851+5G>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.7786+70G>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.7786+70G>A
  variant of: http://identifiers.org/hgnc/12857
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.7849+5G>A
  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.7851+5G>A
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3061
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14341
  bin: 2.25e1
  variant carriers: 0
hgvs: c.7849+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-100390191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390191
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390191
    reference: chr 7
allele count: 1
allele frequency: 1.017004312098283e-5
allele num: 98328
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.7849+25C>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.3099+25C>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.7849+25C>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.7849+25C>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.7851+25C>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.7851+25C>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.7786+90C>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.7786+90C>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.7851+25C>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.7851+25C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9075
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7036
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

7-100390192-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100390192
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100390192
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 97416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.7851+26G>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.7851+26G>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.7849+26G>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.7851+26G>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.7849+26G>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.3099+26G>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.7786+91G>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.7786+91G>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.7851+26G>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.7849+26G>A
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8032
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 151
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6648
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 862
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39757
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1496
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3536
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8344
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15352
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.269632319564231e-4
allele num: 8812
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10778
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 7.644e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

DP
type: SiteQuality
SIO_000300: 1.328163e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.059e1

GenotypeQuality
all individuals: 3482
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 879
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6898
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1187
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38510
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1539
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1587
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62408
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8816
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5394
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.580679126085812e-5
allele num: 15196
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

VQSLOD
type: SiteQuality
SIO_000300: 7.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.353e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.561e0

DP
type: SiteQuality
SIO_000300: 1.322636e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.55e-1

GenotypeQuality
all individuals: 1098
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38201
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7345
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8804
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14962
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10716
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.606374092398638e-5
allele num: 62252
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.9e-1

FS
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SIO_000300: 1.952e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.09e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-1

DP
type: SiteQuality
SIO_000300: 1.31864e6

VQSLOD
type: SiteQuality
SIO_000300: -1.584e0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.607096940087426e-5
allele num: 62224
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14946
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.47e-1

FS
type: SiteQuality
SIO_000300: 1.568e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

DP
type: SiteQuality
SIO_000300: 1.320559e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.303e1

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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14946
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8806
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.855976243504083e-4
allele num: 5388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62224
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

BaseQRankSum
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SIO_000300: -1.47e-1

ReadPosRankSum
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SIO_000300: 9.88e-1

VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.568e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

QD
type: SiteQuality
SIO_000300: 1.303e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.320559e6

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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variant carriers: 0

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: 62098
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.203948952564411e-4
allele num: 8306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14796
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5380
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.61e-1

FS
type: SiteQuality
SIO_000300: 1.044e0

MQRankSum
type: SiteQuality
SIO_000300: 9.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

VQSLOD
type: SiteQuality
SIO_000300: -2.114e0

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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8782
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.614465611882467e-5
allele num: 61940
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10642
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.777e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.312557e6

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.08e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele count: 0
allele frequency: 0.0e0
allele num: 10536
num of homozygotes: 0

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

South Asian
type: Population
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
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allele count: 11
allele frequency: 1.258293296728437e-3
allele num: 8742
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61488
num of homozygotes: 0

East Asian
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allele count: 0
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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DP
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MQ
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QD
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.946279503715586e-4
allele num: 61094
num of homozygotes: 0

African
type: Population
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allele frequency: 1.150483202945237e-4
allele num: 8692
num of homozygotes: 0

Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
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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num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5284
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.246376811594203e-5
allele num: 13800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61094
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

QD
type: SiteQuality
SIO_000300: 1.12e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -9.86e-1

DP
type: SiteQuality
SIO_000300: 1.280606e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

GenotypeQuality
all individuals: 1679
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2991
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8138
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.155268022181146e-4
allele num: 8656
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60818
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.34e-1

InbreedingCoeff
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SIO_000300: -1.9e-3

VQSLOD
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FS
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SIO_000300: 7.89e-1

QD
type: SiteQuality
SIO_000300: 6.69e0

MQRankSum
type: SiteQuality
SIO_000300: 6.72e-1

DP
type: SiteQuality
SIO_000300: 1.268418e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.49e-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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.649076517150396e-5
allele num: 60640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

DP
type: SiteQuality
SIO_000300: 1.256546e6

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

InbreedingCoeff
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SIO_000300: -1.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.826e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 679
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13266
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8082
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60542
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.44e0

DP
type: SiteQuality
SIO_000300: 1.252403e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.026e1

VQSLOD
type: SiteQuality
SIO_000300: -1.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 6.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e-1

GenotypeQuality
all individuals: 478
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 340
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5066
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.084074373484237e-5
allele num: 12370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59292
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.912e0

QD
type: SiteQuality
SIO_000300: 1.277e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.201121e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-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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GenotypeQuality
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GenotypeQuality
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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: 8418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.699466367560586e-5
allele num: 58842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12156
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.84e-1

DP
type: SiteQuality
SIO_000300: 1.182794e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.72e-1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.54e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.55e0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.804337627656887e-5
allele num: 55422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9126
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10558
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

DP
type: SiteQuality
SIO_000300: 1.008593e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -8.407e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.781e0

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9078
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.37324910738808e-4
allele num: 7282
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.272e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.021e0

MQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

DP
type: SiteQuality
SIO_000300: 9.97915e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.22e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 593
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7802
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.54320987654321e-3
allele num: 648
num of homozygotes: 0

East Asian
type: Population
allele count: 23
allele frequency: 3.228523301516002e-3
allele num: 7124
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4588
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.41e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

DP
type: SiteQuality
SIO_000300: 9.38607e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9052
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.824384274131865e-5
allele num: 52296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6774
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.43e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

DP
type: SiteQuality
SIO_000300: 8.6459e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.02e-1

FS
type: SiteQuality
SIO_000300: 2.352e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.974957538412924e-5
allele num: 50634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.195e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.78e-1

DP
type: SiteQuality
SIO_000300: 8.32617e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.021345407503234e-5
allele num: 49472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6248
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.1e-2

DP
type: SiteQuality
SIO_000300: 8.15799e5

QD
type: SiteQuality
SIO_000300: 8.6e0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 247
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GenotypeQuality
all individuals: 140
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.075119319360863e-5
allele num: 48190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

DP
type: SiteQuality
SIO_000300: 7.97687e5

FS
type: SiteQuality
SIO_000300: 1.544e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.850000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

GenotypeQuality
all individuals: 880
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 380
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.708817498291183e-4
allele num: 11704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9362
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.034e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.86e-1

MQ
type: SiteQuality
SIO_000300: 6.079e1

DP
type: SiteQuality
SIO_000300: 1.546593e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.571981010469394e-5
allele num: 63614
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.549494e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

FS
type: SiteQuality
SIO_000300: 2.576e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.489e1

VQSLOD
type: SiteQuality
SIO_000300: 8.139999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56045190687223e-5
allele num: 64084
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9384
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.174e1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.03e-1

FS
type: SiteQuality
SIO_000300: 2.808e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

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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bin: 3.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 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: 1
allele frequency: 1.065870816457045e-4
allele num: 9382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.162e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.803e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

FS
type: SiteQuality
SIO_000300: 9.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.57599e6

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.16e-1

GenotypeQuality
all individuals: 1220
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 143
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 147
bin: 4.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38256
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2521
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64206
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.704735376044568e-5
allele num: 11488
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13786
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.741e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.618e0

DP
type: SiteQuality
SIO_000300: 1.580088e6

GenotypeQuality
all individuals: 8731
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 121
bin: 1.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64318
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.258037044922291e-4
allele num: 9394
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

DP
type: SiteQuality
SIO_000300: 1.585773e6

FS
type: SiteQuality
SIO_000300: 5.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.065e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.255e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeDepth
all individuals: 715
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
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GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 374
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39782
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variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9446
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.356155188615921e-4
allele num: 14898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 1.600035e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.211e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 1213
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2091
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variant carriers: 0

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15082
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.058649163667161e-4
allele num: 9446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-1

QD
type: SiteQuality
SIO_000300: 1.336e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.47e-1

FS
type: SiteQuality
SIO_000300: 1.117e0

DP
type: SiteQuality
SIO_000300: 1.602833e6

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1216
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 370
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 6
allele frequency: 5.211952744961779e-4
allele num: 11512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.632060031498008e-5
allele num: 64766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15192
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.109e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.606262e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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
all individuals: 1050
bin: 8.25e1
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GenotypeQuality
all individuals: 327
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.632060031498008e-5
allele num: 64766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.606262e6

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: -2.81e-1

FS
type: SiteQuality
SIO_000300: 1.109e0

BaseQRankSum
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SIO_000300: -8.73e-1

InbreedingCoeff
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SIO_000300: 2.4e-3

QD
type: SiteQuality
SIO_000300: 1.162e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.05e-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
all individuals: 8862
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15334
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.004811547714515e-4
allele num: 64844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 1.253e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.15e-1

FS
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.38e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 1.609488e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2559
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GenotypeQuality
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GenotypeQuality
all individuals: 216
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GenotypeQuality
all individuals: 2417
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variant carriers: 0

GenotypeQuality
all individuals: 50
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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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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9530
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: 8550
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.064852274120387e-5
allele num: 65256
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

DP
type: SiteQuality
SIO_000300: 1.622098e6

ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.23e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.279e1

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15892
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532426137060194e-5
allele num: 65256
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.279e1

DP
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MQRankSum
type: SiteQuality
SIO_000300: 1.87e-1

BaseQRankSum
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SIO_000300: -2.564e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 4.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9560
num of homozygotes: 0

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

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

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

Latino
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allele count: 1
allele frequency: 8.667013347200555e-5
allele num: 11538
num of homozygotes: 0

DP
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SIO_000300: 1.629364e6

MQ
type: SiteQuality
SIO_000300: 5.937e1

ReadPosRankSum
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FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: -7.768e-1

InbreedingCoeff
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SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

BaseQRankSum
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SIO_000300: -1.605e0

QD
type: SiteQuality
SIO_000300: 2.271e1

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65466
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9570
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.165228113440197e-5
allele num: 16220
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.254e0

DP
type: SiteQuality
SIO_000300: 1.630085e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

QD
type: SiteQuality
SIO_000300: 1.553e1

FS
type: SiteQuality
SIO_000300: 8.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.676e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65510
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.229861025704096e-4
allele num: 16262
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9580
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: 4.67e-1

ClippingRankSum
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

DP
type: SiteQuality
SIO_000300: 1.630912e6

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 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
allele num: 9582
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.052875809012089e-5
allele num: 65512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.631156e6

QD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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FS
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MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 16312
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: 2
allele frequency: 3.053621595211921e-5
allele num: 65496
num of homozygotes: 0

Latino
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: 8552
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Other
type: Population
allele count: 0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

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

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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bin: 3.75e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527043948324833e-5
allele num: 65486
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQ
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -4.622e0

DP
type: SiteQuality
SIO_000300: 1.62935e6

QD
type: SiteQuality
SIO_000300: 1.374e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.018e0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 41625
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1204
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 369
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8959
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2542
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 323
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.838911364472232e-4
allele num: 16314
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.679457182966776e-4
allele num: 8548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.527557130636686e-4
allele num: 65464
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.91e-1

FS
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.74e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

QD
type: SiteQuality
SIO_000300: 1.179e1

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-1

DP
type: SiteQuality
SIO_000300: 1.627637e6

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1043
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2540
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41678
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8954
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1164
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 3
allele frequency: 3.130217028380634e-4
allele num: 9584
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65464
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
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: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.626726e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.58e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.991e0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

QD
type: SiteQuality
SIO_000300: 1.353e1

MQRankSum
type: SiteQuality
SIO_000300: -4.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1255
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2542
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8961
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41649
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
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: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.055114261273371e-5
allele num: 65464
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 1.625689e6

FS
type: SiteQuality
SIO_000300: 1.464e0

MQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-2

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 9.71e-1

QD
type: SiteQuality
SIO_000300: 1.387e1

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

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1454
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8880
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1032
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41202
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2512
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 9.75e1
variant carriers: 5

African
type: Population
allele count: 1
allele frequency: 1.046462955211386e-4
allele num: 9556
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.120700208103807e-5
allele num: 65352
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.51e0

DP
type: SiteQuality
SIO_000300: 1.619431e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.956e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 1.292e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 259
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2513
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8862
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2369
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1475
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41214
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.688097306689835e-5
allele num: 11510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16308
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.864e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.643e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.889e0

VQSLOD
type: SiteQuality
SIO_000300: -5.144e0

QD
type: SiteQuality
SIO_000300: 7.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e0

DP
type: SiteQuality
SIO_000300: 1.6183e6

GenotypeQuality
all individuals: 40277
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8733
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variant carriers: 0

GenotypeQuality
all individuals: 355
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variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16234
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537515375153751e-5
allele num: 65040
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.344665885111372e-4
allele num: 8530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9486
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.357e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.274e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.604492e6

GenotypeQuality
all individuals: 318
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1119
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 301
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variant carriers: 0

GenotypeQuality
all individuals: 2263
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variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40697
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8581
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64990
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9452
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.345215759849906e-4
allele num: 8528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.867e1

DP
type: SiteQuality
SIO_000300: 1.599192e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

QD
type: SiteQuality
SIO_000300: 1.304e1

VQSLOD
type: SiteQuality
SIO_000300: -8.393e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

FS
type: SiteQuality
SIO_000300: 1.006e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

GenotypeQuality
all individuals: 605
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38693
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variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 187
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variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2297
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9328
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15770
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.176470588235294e-4
allele num: 8500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64326
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.33e-1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

FS
type: SiteQuality
SIO_000300: 4.775e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 1.562045e6

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: 6.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15598
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.826125330979699e-5
allele num: 11330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.355703860787127e-5
allele num: 64132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9284
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
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QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 3.0e-3

FS
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MQ
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SIO_000300: 6.0e1

MQRankSum
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VQSLOD
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SIO_000300: 1.09e0

DP
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SIO_000300: 1.55049e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.411900487304436e-5
allele num: 15596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.120514260750172e-5
allele num: 64092
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.829242450997704e-5
allele num: 11326
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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VQSLOD
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SIO_000300: 1.64e0

ReadPosRankSum
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SIO_000300: -4.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

FS
type: SiteQuality
SIO_000300: 1.353e0

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

DP
type: SiteQuality
SIO_000300: 1.548995e6

QD
type: SiteQuality
SIO_000300: 1.265e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.74e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563966218329684e-5
allele num: 63940
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.480041472265422e-5
allele num: 15432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

FS
type: SiteQuality
SIO_000300: 2.323e0

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

QD
type: SiteQuality
SIO_000300: 1.103e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.534016e6

VQSLOD
type: SiteQuality
SIO_000300: -1.222e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.619e0

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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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.571289400081707e-5
allele num: 63642
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.422e1

DP
type: SiteQuality
SIO_000300: 1.519557e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.508e0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

South Asian
type: Population
allele count: 20
allele frequency: 1.326084073730274e-3
allele num: 15082
num of homozygotes: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63598
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

FS
type: SiteQuality
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QD
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.49e-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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variant carriers: 0

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

Latino
type: Population
allele count: 0
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
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14696
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.584836286411614e-5
allele num: 63098
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

ReadPosRankSum
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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SIO_000300: 1.4e-3

VQSLOD
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6182
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10992
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South Asian
type: Population
allele count: 1
allele frequency: 7.087172218284904e-5
allele num: 14110
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

MQ
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FS
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
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MQRankSum
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SIO_000300: 1.91e-1

ReadPosRankSum
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DP
type: SiteQuality
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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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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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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: 2061
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 584
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 685
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 5524
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 31244
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 771
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2320
bin: 9.75e1
variant carriers: 1623

GenotypeQuality
all individuals: 569
bin: 4.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 75
allele frequency: 1.225890813991501e-2
allele num: 6118
num of homozygotes: 1

Latino
type: Population
allele count: 67
allele frequency: 6.137779406375962e-3
allele num: 10916
num of homozygotes: 0

African
type: Population
allele count: 27
allele frequency: 3.041910770617395e-3
allele num: 8876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1324
allele frequency: 2.141632428585293e-2
allele num: 61822
num of homozygotes: 16

South Asian
type: Population
allele count: 176
allele frequency: 1.266916210768788e-2
allele num: 13892
num of homozygotes: 3

East Asian
type: Population
allele count: 3
allele frequency: 3.648747263439553e-4
allele num: 8222
num of homozygotes: 0

Other
type: Population
allele count: 11
allele frequency: 1.354679802955665e-2
allele num: 812
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 6.49e-1

DP
type: SiteQuality
SIO_000300: 1.385457e6

QD
type: SiteQuality
SIO_000300: 1.444e1

VQSLOD
type: SiteQuality
SIO_000300: 4.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

GenotypeQuality
all individuals: 413
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32377
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.623007757977083e-5
allele num: 61614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8210
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10894
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.113e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.82e0

DP
type: SiteQuality
SIO_000300: 1.355388e6

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

FS
type: SiteQuality
SIO_000300: 1.0004e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.292e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e-1

QD
type: SiteQuality
SIO_000300: 1.654e1

GenotypeQuality
all individuals: 771
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10147
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1292
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1429
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5451
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30240
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2346
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1367
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2574
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.909662215239592e-5
allele num: 61104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10780
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.429420505200594e-5
allele num: 13460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8734
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

DP
type: SiteQuality
SIO_000300: 1.323442e6

VQSLOD
type: SiteQuality
SIO_000300: 5.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

QD
type: SiteQuality
SIO_000300: 1.442e1

FS
type: SiteQuality
SIO_000300: 6.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

GenotypeQuality
all individuals: 1300
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1498
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2813
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10799
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 4956
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2543
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.790750568612585e-4
allele num: 13190
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.869158878504673e-4
allele num: 10700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.651145895251304e-5
allele num: 60564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5924
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.234872808100766e-4
allele num: 8098
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.94e1

DP
type: SiteQuality
SIO_000300: 1.298874e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.84e0

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 4.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

QD
type: SiteQuality
SIO_000300: 9.07e0

GenotypeQuality
all individuals: 1187
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10955
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28988
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2778
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2548
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.647555028337947e-5
allele num: 60696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8680
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.873e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.15e-1

MQ
type: SiteQuality
SIO_000300: 5.828e1

QD
type: SiteQuality
SIO_000300: 1.047e1

MQRankSum
type: SiteQuality
SIO_000300: 6.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.294518e6

VQSLOD
type: SiteQuality
SIO_000300: -3.22e-2

GenotypeQuality
all individuals: 12232
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2856
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1079
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3074
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4773
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27558
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1602
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5844
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.729487817006464e-4
allele num: 8044
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.626e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.32e-1

QD
type: SiteQuality
SIO_000300: 9.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.257138e6

VQSLOD
type: SiteQuality
SIO_000300: 4.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 27185
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4738
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2930
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12447
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3154
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60038
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.735059760956175e-4
allele num: 8032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12830
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.82e-1

FS
type: SiteQuality
SIO_000300: 2.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.148e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.641e0

DP
type: SiteQuality
SIO_000300: 1.249919e6

GenotypeQuality
all individuals: 1055
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25824
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13035
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4281
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3367
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1740
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 163
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3087
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 962
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 851
bin: 9.75e1
variant carriers: 174

GenotypeQuality
all individuals: 694
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5756
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.655257653546302e-4
allele num: 10518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.848553087083655e-4
allele num: 59506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7976
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12458
num of homozygotes: 0

African
type: Population
allele count: 156
allele frequency: 1.829697396199859e-2
allele num: 8526
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.31e0

QD
type: SiteQuality
SIO_000300: 1.304e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

DP
type: SiteQuality
SIO_000300: 1.225251e6

GenotypeQuality
all individuals: 1067
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26184
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 537
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 655
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3166
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13347
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4225
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3435
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 131
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 732
bin: 9.75e1
variant carriers: 64

GenotypeQuality
all individuals: 155
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1166
bin: 5.25e1
variant carriers: 1

African
type: Population
allele count: 65
allele frequency: 7.665094339622642e-3
allele num: 8480
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5758
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.603849238171612e-4
allele num: 12470
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.540164090822362e-5
allele num: 10482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.682708487581611e-5
allele num: 59428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.347708894878706e-3
allele num: 742
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.42e-1

DP
type: SiteQuality
SIO_000300: 1.215407e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.49e0

QD
type: SiteQuality
SIO_000300: 1.35e1

GenotypeQuality
all individuals: 4070
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14192
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 988
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25216
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3705
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5688
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.691303318337111e-5
allele num: 59126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQRankSum
type: SiteQuality
SIO_000300: -1.397e0

DP
type: SiteQuality
SIO_000300: 1.187709e6

VQSLOD
type: SiteQuality
SIO_000300: -1.211e0

QD
type: SiteQuality
SIO_000300: 8.789999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

FS
type: SiteQuality
SIO_000300: 5.825e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-2

GenotypeQuality
all individuals: 1224
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25021
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4012
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1908
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3499
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 850
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.694226077527785e-5
allele num: 59024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5668
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12210
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.182839e6

FS
type: SiteQuality
SIO_000300: 1.642e0

VQSLOD
type: SiteQuality
SIO_000300: -4.544e-1

QD
type: SiteQuality
SIO_000300: 1.842e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.261e0

GenotypeQuality
all individuals: 137
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2272
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5704
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17930
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1059
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3988
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14240
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.770287494689137e-5
allele num: 56488
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10454
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

MQ
type: SiteQuality
SIO_000300: 5.836e1

FS
type: SiteQuality
SIO_000300: 1.935e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

DP
type: SiteQuality
SIO_000300: 1.003691e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

QD
type: SiteQuality
SIO_000300: 1.268e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.897e0