10-75555351-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555351
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555351
    reference: chr 10
allele count: 1
allele frequency: 8.290224167661493e-6
allele num: 120624
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2849G>A
  hgvsp: ENSP00000474043.1:p.Arg950His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1805G>A
  hgvsp: ENSP00000432423.1:p.Arg602His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.580G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.2948G>A
  hgvsp: ENSP00000474348.1:p.Arg983His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.966G>A
  hgvsp: ENSP00000474766.1:p.Arg323His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.744G>A
  hgvsp: ENSP00000474118.1:p.Arg249His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.2963G>A
  hgvsp: ENSP00000474944.1:p.Arg988His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.484G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.772G>A
  hgvsp: ENSP00000415612.1:p.Arg258His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.2963G>A
  hgvsp: ENSP00000381693.2:p.Arg988His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.2942G>A
  hgvsp: ENSP00000387828.2:p.Arg981His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.2948G>A
  hgvsp: ENSP00000474748.1:p.Arg983His
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14770
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg988His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

10-75555373-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555373
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555373
    reference: chr 10
allele count: 4
allele frequency: 3.321155762205247e-5
allele num: 120440
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.602A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2871A>G
  hgvsp: ENST00000603114.1:c.2871A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.2985A>G
  hgvsp: ENST00000604729.1:c.2985A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.2970A>G
  hgvsp: ENST00000604524.1:c.2970A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1827A>G
  hgvsp: ENST00000492395.1:c.1827A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.2964A>G
  hgvsp: ENST00000433366.2:c.2964A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.988A>G
  hgvsp: ENST00000603187.1:c.988A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.2985A>G
  hgvsp: ENST00000398706.2:c.2985A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.794A>G
  hgvsp: ENST00000412198.1:c.794A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.2970A>G
  hgvsp: ENST00000605216.1:c.2970A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.766A>G
  hgvsp: ENST00000604754.1:c.766A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.506A>G
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28077
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala995Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

10-75555375-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555375
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555375
    reference: chr 10
allele count: 1
allele frequency: 8.303165166561494e-6
allele num: 120436
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.508T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.990T>C
  hgvsp: ENSP00000474766.1:p.Leu331Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.2987T>C
  hgvsp: ENSP00000381693.2:p.Leu996Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.768T>C
  hgvsp: ENSP00000474118.1:p.Leu257Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.2972T>C
  hgvsp: ENSP00000474748.1:p.Leu991Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.2966T>C
  hgvsp: ENSP00000387828.2:p.Leu989Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.2987T>C
  hgvsp: ENSP00000474944.1:p.Leu996Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1829T>C
  hgvsp: ENSP00000432423.1:p.Leu610Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2873T>C
  hgvsp: ENSP00000474043.1:p.Leu958Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.796T>C
  hgvsp: ENSP00000415612.1:p.Leu266Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.2972T>C
  hgvsp: ENSP00000474348.1:p.Leu991Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.604T>C
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28078
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu996Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

10-75555400-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555400
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555400
    reference: chr 10
allele count: 10
allele frequency: 8.349057391420509e-5
allele num: 119774
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3012C>T
  hgvsp: ENST00000398706.2:c.3012C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3012C>T
  hgvsp: ENST00000604729.1:c.3012C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.793C>T
  hgvsp: ENST00000604754.1:c.793C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1854C>T
  hgvsp: ENST00000492395.1:c.1854C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2898C>T
  hgvsp: ENST00000603114.1:c.2898C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.2991C>T
  hgvsp: ENST00000433366.2:c.2991C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.533C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1015C>T
  hgvsp: ENST00000603187.1:c.1015C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.629C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.2997C>T
  hgvsp: ENST00000604524.1:c.2997C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.2997C>T
  hgvsp: ENST00000605216.1:c.2997C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.821C>T
  hgvsp: ENST00000412198.1:c.821C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10901
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp1004Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

10-75555401-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555401
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555401
    reference: chr 10
allele count: 1
allele frequency: 8.356173541012099e-6
allele num: 119672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.630G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2899G>A
  hgvsp: ENSP00000474043.1:p.Asp967Asn
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.2992G>A
  hgvsp: ENSP00000387828.2:p.Asp998Asn
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3013G>A
  hgvsp: ENSP00000381693.2:p.Asp1005Asn
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1855G>A
  hgvsp: ENSP00000432423.1:p.Asp619Asn
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.794G>A
  hgvsp: ENSP00000474118.1:p.Asp266Asn
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.822G>A
  hgvsp: ENSP00000415612.1:p.Asp275Asn
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1016G>A
  hgvsp: ENSP00000474766.1:p.Asp340Asn
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.2998G>A
  hgvsp: ENSP00000474748.1:p.Asp1000Asn
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3013G>A
  hgvsp: ENSP00000474944.1:p.Asp1005Asn
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.534G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.2998G>A
  hgvsp: ENSP00000474348.1:p.Asp1000Asn
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp1005Asn
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: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

10-75555403-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555403
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555403
    reference: chr 10
allele count: 1
allele frequency: 8.373386029842748e-6
allele num: 119426
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.632C>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3000C>G
  hgvsp: ENSP00000474748.1:p.Asp1000Glu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1018C>G
  hgvsp: ENSP00000474766.1:p.Asp340Glu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3015C>G
  hgvsp: ENSP00000381693.2:p.Asp1005Glu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.536C>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.824C>G
  hgvsp: ENSP00000415612.1:p.Asp275Glu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1857C>G
  hgvsp: ENSP00000432423.1:p.Asp619Glu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3000C>G
  hgvsp: ENSP00000474348.1:p.Asp1000Glu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.796C>G
  hgvsp: ENSP00000474118.1:p.Asp266Glu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.2994C>G
  hgvsp: ENSP00000387828.2:p.Asp998Glu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3015C>G
  hgvsp: ENSP00000474944.1:p.Asp1005Glu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2901C>G
  hgvsp: ENSP00000474043.1:p.Asp967Glu
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp1005Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

10-75555412-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555412
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555412
    reference: chr 10
allele count: 1
allele frequency: 8.454514710855598e-6
allele num: 118280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3009G>A
  hgvsp: ENST00000604524.1:c.3009G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3024G>A
  hgvsp: ENST00000398706.2:c.3024G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.641G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3003G>A
  hgvsp: ENST00000433366.2:c.3003G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.833G>A
  hgvsp: ENST00000412198.1:c.833G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.545G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1866G>A
  hgvsp: ENST00000492395.1:c.1866G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3024G>A
  hgvsp: ENST00000604729.1:c.3024G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1027G>A
  hgvsp: ENST00000603187.1:c.1027G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2910G>A
  hgvsp: ENST00000603114.1:c.2910G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3009G>A
  hgvsp: ENST00000605216.1:c.3009G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.805G>A
  hgvsp: ENST00000604754.1:c.805G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys1008Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

10-75555421-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555421
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555421
    reference: chr 10
allele count: 2
allele frequency: 1.714648239913582e-5
allele num: 116642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.814G>A
  hgvsp: ENST00000604754.1:c.814G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1875G>A
  hgvsp: ENST00000492395.1:c.1875G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1036G>A
  hgvsp: ENST00000603187.1:c.1036G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3018G>A
  hgvsp: ENST00000605216.1:c.3018G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3018G>A
  hgvsp: ENST00000604524.1:c.3018G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.842G>A
  hgvsp: ENST00000412198.1:c.842G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3033G>A
  hgvsp: ENST00000604729.1:c.3033G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3012G>A
  hgvsp: ENST00000433366.2:c.3012G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3033G>A
  hgvsp: ENST00000398706.2:c.3033G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.554G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2919G>A
  hgvsp: ENST00000603114.1:c.2919G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.650G>A
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26066
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3033G>A
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

10-75555430-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555430
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555428
    reference: chr 10
allele count: 5
allele frequency: 4.400014080045056e-5
allele num: 113636
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3033+10_3033+11delTG
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.842+10_842+11delTG
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.650+10_650+11delTG
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.814+10_814+11delTG
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.554+10_554+11delTG
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1036+10_1036+11delTG
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3018+10_3018+11delTG
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3018+10_3018+11delTG
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3012+10_3012+11delTG
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3033+10_3033+11delTG
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1875+10_1875+11delTG
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2919+10_2919+11delTG
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22672
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9635
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: CTG
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

10-75555433-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555433
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555433
    reference: chr 10
allele count: 1
allele frequency: 8.865091044485026e-6
allele num: 112802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3018+12G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2919+12G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3033+12G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3012+12G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3018+12G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1036+12G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.842+12G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3033+12G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.554+12G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.814+12G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.650+12G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1875+12G>C
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21573
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

10-75555437-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555437
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555437
    reference: chr 10
allele count: 4
allele frequency: 3.609977979134327e-5
allele num: 110804
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.554+16T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1036+16T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3012+16T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3018+16T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3033+16T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.814+16T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2919+16T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3033+16T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3018+16T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.842+16T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.650+16T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1875+16T>G
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8777
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

10-75555443-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555443
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555443
    reference: chr 10
allele count: 1
allele frequency: 9.159522239319997e-6
allele num: 109176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3033+22C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.814+22C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3033+22C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3018+22C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.650+22C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.554+22C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2919+22C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1875+22C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3018+22C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3012+22C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1036+22C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.842+22C>T
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

10-75555444-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555444
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555444
    reference: chr 10
allele count: 1
allele frequency: 9.218289085545723e-6
allele num: 108480
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3018+23G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3012+23G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3018+23G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2919+23G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3033+23G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1875+23G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.842+23G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1036+23G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3033+23G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.814+23G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.650+23G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.554+23G>A
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14240
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

10-75555454-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555454
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555454
    reference: chr 10
allele count: 1
allele frequency: 9.451438508941061e-6
allele num: 105804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1036+33G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3033+33G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3018+33G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3018+33G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.814+33G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.650+33G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.842+33G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3012+33G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3033+33G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2919+33G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1875+33G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.554+33G>A
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8237
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

10-75555457-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555457
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555457
    reference: chr 10
allele count: 3
allele frequency: 2.864344637946838e-5
allele num: 104736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3018+36T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.650+36T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.814+36T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.842+36T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3033+36T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3033+36T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1036+36T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3018+36T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3012+36T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1875+36T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2919+36T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.554+36T>C
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14608
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15423
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8009
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-75555463-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555463
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555463
    reference: chr 10
allele count: 3
allele frequency: 2.910247953125606e-5
allele num: 103084
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3033+42C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.554+42C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3033+42C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1036+42C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.842+42C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.814+42C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2919+42C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3018+42C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3018+42C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3012+42C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.650+42C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1875+42C>T
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15538
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

10-75555464-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75555464
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75555464
    reference: chr 10
allele count: 17
allele frequency: 1.65614527316655e-4
allele num: 102648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3033+43C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3018+43C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.842+43C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1875+43C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1036+43C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.650+43C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2919+43C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3018+43C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3033+43C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.554+43C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.814+43C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3012+43C>T
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15481
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6224
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9360
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15127
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-75556037-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556037
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556037
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 1700
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.651-42T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-495T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-495T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-495T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-495T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.555-42T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-495T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-474T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-495T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-495T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-495T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-495T>A
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

10-75556052-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556052
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556052
    reference: chr 10
allele count: 1
allele frequency: 4.464285714285714e-4
allele num: 2240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-480A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-480A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-459A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-480A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-480A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-480A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-480A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-480A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-480A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.555-27A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-480A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.651-27A>G
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

10-75556093-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556093
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556093
    reference: chr 10
allele count: 1
allele frequency: 1.874765654293213e-4
allele num: 5334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  hgvsc: ENST00000425051.1:n.569C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-439C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-439C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-439C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-418C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-439C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.665C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-439C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-439C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-439C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-439C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-439C>T
  variant of: http://identifiers.org/hgnc/23528
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

10-75556108-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556108
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556107
    reference: chr 10
allele count: 582
allele frequency: 1.665712650257584e-1
allele num: 3494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000489234
  gene symbol: ZSWIM8
  hgvsc: ENST00000489234.1:n.681delA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-414delA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-414delA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-414delA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-414delA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-414delA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-414delA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-414delA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-414delA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-414delA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-393delA
  variant of: http://identifiers.org/hgnc/23528
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.75e1
  variant carriers: 250
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 7.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 2.25e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 1.25e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 2.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: TA
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

10-75556108-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556108
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556109
    reference: chr 10
allele count: 176
allele frequency: 5.037206639954207e-2
allele num: 3494
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-414dupA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-414dupA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-414dupA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-414dupA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-414dupA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-414dupA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-393dupA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-414dupA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-414dupA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-414dupA
  variant of: http://identifiers.org/hgnc/23528
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 1.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 2.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 2.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 2.5e0
  variant carriers: 10
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

10-75556116-AAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556116
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556113
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 7600
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-404_2920-402delGAA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000425051
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-404_843-402delGAA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-404_3019-402delGAA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-383_815-381delGAA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-404_3034-402delGAA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-404_3019-402delGAA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-404_1037-402delGAA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-404_3013-402delGAA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-404_1876-402delGAA
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-404_3034-402delGAA
  variant of: http://identifiers.org/hgnc/23528
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: AAAG
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

10-75556122-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556122
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556122
    reference: chr 10
allele count: 1
allele frequency: 1.322051824431518e-4
allele num: 7564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-410G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-410G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-410G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-410G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-410G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-410G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-410G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-389G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-410G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-410G>A
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/10-75556140-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556140
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556140
    reference: chr 10
allele count: 1
allele frequency: 1.478852410529429e-4
allele num: 6762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-392A>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-392A>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-392A>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-392A>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-371A>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-392A>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-392A>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-392A>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.12A>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-392A>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-392A>C
  variant of: http://identifiers.org/hgnc/23528
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

10-75556141-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556141
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556141
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 6376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-391G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-370G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-391G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-391G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-391G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-391G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-391G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-391G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-391G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-391G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.13G>T
  variant of: http://identifiers.org/hgnc/23528
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

10-75556462-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556462
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556461
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 100794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-69delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-69delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-69delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1269delA
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-69delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-69delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-48delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-69delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2555delA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-69delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-69delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-69delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-69delT
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8487
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: GT
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS

10-75556465-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556465
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556465
    reference: chr 10
allele count: 2
allele frequency: 1.974099810486418e-5
allele num: 101312
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1267T>C
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-67A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2553T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-67A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-67A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-67A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-46A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-67A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-67A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-67A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-67A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-67A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-67A>G
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18996
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11148
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14093
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

10-75556465-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556465
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556464
    reference: chr 10
allele count: 1
allele frequency: 9.87049905243209e-6
allele num: 101312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-66delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-66delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-45delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1266delA
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-66delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-66delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-66delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-66delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2552delA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-66delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-66delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-66delT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-66delT
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14093
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18996
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: AT
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

10-75556485-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556485
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556485
    reference: chr 10
allele count: 2
allele frequency: 1.877722697911972e-5
allele num: 106512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-26G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-47G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-47G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2533C>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-47G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1247C>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-47G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-47G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-47G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-47G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-47G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-47G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-47G>T
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34324
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

10-75556488-ATCCTGTCACTGCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556488
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556475
    reference: chr 10
allele count: 1
allele frequency: 9.234292468511062e-6
allele num: 108292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5932
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8208
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: ATCCTGTCACTGCT
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum

10-75556491-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556491
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556491
    reference: chr 10
allele count: 1
allele frequency: 9.138595946118838e-6
allele num: 109426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-41C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-41C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-41C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-41C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-41C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-41C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2527G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-41C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-20C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-41C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1241G>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-41C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-41C>T
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

10-75556492-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556492
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556492
    reference: chr 10
allele count: 1
allele frequency: 9.085457816219359e-6
allele num: 110066
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-40T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-40T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1240A>G
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-19T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-40T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-40T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2526A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-40T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-40T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-40T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-40T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-40T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-40T>C
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: T
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

10-75556493-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556493
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556493
    reference: chr 10
allele count: 1
allele frequency: 9.050920478612675e-6
allele num: 110486
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-18G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-39G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2525C>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-39G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-39G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1239C>G
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-39G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-39G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-39G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-39G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-39G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-39G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-39G>C
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP

10-75556497-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556497
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556497
    reference: chr 10
allele count: 1
allele frequency: 8.8974304220941e-6
allele num: 112392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-35C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1235G>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-35C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-35C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-35C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-35C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-14C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-35C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-35C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2521G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-35C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-35C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-35C>T
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

10-75556499-GCTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556499
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556496
    reference: chr 10
allele count: 12
allele frequency: 1.058817301074699e-4
allele num: 113334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-30_3019-28delTCT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-30_843-28delTCT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-30_3019-28delTCT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-30_3034-28delTCT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-9_815-7delTCT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-30_1037-28delTCT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-30_1876-28delTCT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-30_3013-28delTCT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2516_*2518delAAG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-30_3034-28delTCT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1230_1232delAAG
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-30_2920-28delTCT
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-30_34-28delTCT
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10108
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 40214
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GCTT
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

10-75556502-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556502
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556502
    reference: chr 10
allele count: 2
allele frequency: 1.748282312627843e-5
allele num: 114398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-30T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-30T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-30T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-30T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-30T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-30T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-30T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1230A>C
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2516A>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-30T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-9T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-30T>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-30T>G
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10458
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

10-75556508-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556508
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556508
    reference: chr 10
allele count: 1
allele frequency: 8.598008701184805e-6
allele num: 116306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-24G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-24G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-24G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-24G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-24G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-24G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1224C>T
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-24G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-24G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2510C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-24G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815-3G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-24G>A
  variant of: http://identifiers.org/hgnc/23528
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11283
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.815-3G>A
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ

10-75556511-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556511
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556511
    reference: chr 10
allele count: 2
allele frequency: 1.709547824600393e-5
allele num: 116990
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-21G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2507C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-21G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-21G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-21G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-21G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.815G>T
  hgvsp: ENSP00000474118.1:p.Val273Phe
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1221C>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-21G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-21G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-21G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-21G>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-21G>T
  variant of: http://identifiers.org/hgnc/23528
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val273Phe
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

10-75556518-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556518
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556518
    reference: chr 10
allele count: 1
allele frequency: 8.460380040271409e-6
allele num: 118198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.822C>T
  hgvsp: ENSP00000474118.1:p.Ala275Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-14C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-14C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-14C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-14C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-14C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2500G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-14C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-14C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1214G>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-14C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-14C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-14C>T
  variant of: http://identifiers.org/hgnc/23528
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala275Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

10-75556529-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556529
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556529
    reference: chr 10
allele count: 1
allele frequency: 8.388276544701125e-6
allele num: 119214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1037-3C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1876-3C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2489G>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2920-3C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1203G>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3013-3C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3019-3C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.833C>T
  hgvsp: ENSP00000474118.1:p.Gln279Ter
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.843-3C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3034-3C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.34-3C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3019-3C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3034-3C>T
  variant of: http://identifiers.org/hgnc/23528
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12795
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln279Ter
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

10-75556537-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556537
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556537
    reference: chr 10
allele count: 2
allele frequency: 1.672073036150219e-5
allele num: 119612
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3039A>G
  hgvsp: ENST00000604729.1:c.3039A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1195T>C
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2481T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1042A>G
  hgvsp: ENST00000603187.1:c.1042A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3024A>G
  hgvsp: ENST00000605216.1:c.3024A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3018A>G
  hgvsp: ENST00000433366.2:c.3018A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1881A>G
  hgvsp: ENST00000492395.1:c.1881A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2925A>G
  hgvsp: ENST00000603114.1:c.2925A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3039A>G
  hgvsp: ENST00000398706.2:c.3039A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3024A>G
  hgvsp: ENST00000604524.1:c.3024A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.841A>G
  hgvsp: ENST00000604754.1:c.841A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.39A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.848A>G
  hgvsp: ENST00000412198.1:c.848A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1013Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

10-75556543-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556543
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556543
    reference: chr 10
allele count: 2
allele frequency: 1.668891855807744e-5
allele num: 119840
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.45A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3030A>G
  hgvsp: ENST00000604524.1:c.3030A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1189T>C
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3030A>G
  hgvsp: ENST00000605216.1:c.3030A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2931A>G
  hgvsp: ENST00000603114.1:c.2931A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2475T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1887A>G
  hgvsp: ENST00000492395.1:c.1887A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1048A>G
  hgvsp: ENST00000603187.1:c.1048A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3024A>G
  hgvsp: ENST00000433366.2:c.3024A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3045A>G
  hgvsp: ENST00000398706.2:c.3045A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.847A>G
  hgvsp: ENST00000604754.1:c.847A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.854A>G
  hgvsp: ENST00000412198.1:c.854A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3045A>G
  hgvsp: ENST00000604729.1:c.3045A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys1015Lys
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/10-75556553-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556553
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556553
    reference: chr 10
allele count: 1
allele frequency: 8.324453915823122e-6
allele num: 120128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2941C>A
  hgvsp: ENST00000603114.1:c.2941C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1897C>A
  hgvsp: ENST00000492395.1:c.1897C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3034C>A
  hgvsp: ENST00000433366.2:c.3034C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.55C>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3040C>A
  hgvsp: ENST00000604524.1:c.3040C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1058C>A
  hgvsp: ENST00000603187.1:c.1058C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3040C>A
  hgvsp: ENST00000605216.1:c.3040C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2465G>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3055C>A
  hgvsp: ENST00000398706.2:c.3055C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1179G>T
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3055C>A
  hgvsp: ENST00000604729.1:c.3055C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.857C>A
  hgvsp: ENST00000604754.1:c.857C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.864C>A
  hgvsp: ENST00000412198.1:c.864C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1019Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

10-75556569-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556569
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556569
    reference: chr 10
allele count: 7
allele frequency: 5.810768183553866e-5
allele num: 120466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2957A>G
  hgvsp: ENSP00000474043.1:p.His986Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1074A>G
  hgvsp: ENSP00000474766.1:p.His359Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1913A>G
  hgvsp: ENSP00000432423.1:p.His638Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3050A>G
  hgvsp: ENSP00000387828.2:p.His1017Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3056A>G
  hgvsp: ENSP00000474748.1:p.His1019Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3071A>G
  hgvsp: ENSP00000381693.2:p.His1024Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.873A>G
  hgvsp: ENSP00000474118.1:p.His292Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.880A>G
  hgvsp: ENSP00000415612.1:p.His294Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3071A>G
  hgvsp: ENSP00000474944.1:p.His1024Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2449T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3056A>G
  hgvsp: ENSP00000474348.1:p.His1019Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.71A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1163T>C
  variant of: http://identifiers.org/hgnc/45103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His1024Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

10-75556581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556581
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556581
    reference: chr 10
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2437G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3062C>T
  hgvsp: ENSP00000387828.2:p.Thr1021Met
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3068C>T
  hgvsp: ENSP00000474748.1:p.Thr1023Met
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3083C>T
  hgvsp: ENSP00000474944.1:p.Thr1028Met
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.892C>T
  hgvsp: ENSP00000415612.1:p.Thr298Met
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.885C>T
  hgvsp: ENSP00000474118.1:p.Thr296Met
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.83C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2969C>T
  hgvsp: ENSP00000474043.1:p.Thr990Met
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3068C>T
  hgvsp: ENSP00000474348.1:p.Thr1023Met
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3083C>T
  hgvsp: ENSP00000381693.2:p.Thr1028Met
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1925C>T
  hgvsp: ENSP00000432423.1:p.Thr642Met
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1086C>T
  hgvsp: ENSP00000474766.1:p.Thr363Met
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1151G>A
  variant of: http://identifiers.org/hgnc/45103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1028Met
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

10-75556607-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556607
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556607
    reference: chr 10
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3088C>T
  hgvsp: ENSP00000387828.2:p.Arg1030Cys
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.911C>T
  hgvsp: ENSP00000474118.1:p.Arg305Cys
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1125G>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3109C>T
  hgvsp: ENSP00000381693.2:p.Arg1037Cys
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1951C>T
  hgvsp: ENSP00000432423.1:p.Arg651Cys
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3094C>T
  hgvsp: ENSP00000474748.1:p.Arg1032Cys
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.109C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1112C>T
  hgvsp: ENSP00000474766.1:p.Arg372Cys
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2995C>T
  hgvsp: ENSP00000474043.1:p.Arg999Cys
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.918C>T
  hgvsp: ENSP00000415612.1:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3109C>T
  hgvsp: ENSP00000474944.1:p.Arg1037Cys
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3094C>T
  hgvsp: ENSP00000474348.1:p.Arg1032Cys
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2411G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1037Cys
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

10-75556608-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556608
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556608
    reference: chr 10
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3089G>A
  hgvsp: ENSP00000387828.2:p.Arg1030His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3095G>A
  hgvsp: ENSP00000474348.1:p.Arg1032His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1124C>T
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3095G>A
  hgvsp: ENSP00000474748.1:p.Arg1032His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3110G>A
  hgvsp: ENSP00000474944.1:p.Arg1037His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.110G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1952G>A
  hgvsp: ENSP00000432423.1:p.Arg651His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3110G>A
  hgvsp: ENSP00000381693.2:p.Arg1037His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.912G>A
  hgvsp: ENSP00000474118.1:p.Arg305His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1113G>A
  hgvsp: ENSP00000474766.1:p.Arg372His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.2996G>A
  hgvsp: ENSP00000474043.1:p.Arg999His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.919G>A
  hgvsp: ENSP00000415612.1:p.Arg307His
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2410C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1037His
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

10-75556612-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556612
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556612
    reference: chr 10
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1120T>C
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3099A>G
  hgvsp: ENST00000605216.1:c.3099A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3114A>G
  hgvsp: ENST00000398706.2:c.3114A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2406T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3099A>G
  hgvsp: ENST00000604524.1:c.3099A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3000A>G
  hgvsp: ENST00000603114.1:c.3000A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3093A>G
  hgvsp: ENST00000433366.2:c.3093A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.923A>G
  hgvsp: ENST00000412198.1:c.923A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.114A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.916A>G
  hgvsp: ENST00000604754.1:c.916A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3114A>G
  hgvsp: ENST00000604729.1:c.3114A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1956A>G
  hgvsp: ENST00000492395.1:c.1956A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1117A>G
  hgvsp: ENST00000603187.1:c.1117A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1038Pro
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

10-75556620-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556620
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556620
    reference: chr 10
allele count: 1
allele frequency: 8.28363154406892e-6
allele num: 120720
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2398G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1964C>T
  hgvsp: ENSP00000432423.1:p.Ala655Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1112G>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.924C>T
  hgvsp: ENSP00000474118.1:p.Ala309Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3101C>T
  hgvsp: ENSP00000387828.2:p.Ala1034Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1125C>T
  hgvsp: ENSP00000474766.1:p.Ala376Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.122C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3122C>T
  hgvsp: ENSP00000381693.2:p.Ala1041Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3122C>T
  hgvsp: ENSP00000474944.1:p.Ala1041Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3107C>T
  hgvsp: ENSP00000474348.1:p.Ala1036Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3008C>T
  hgvsp: ENSP00000474043.1:p.Ala1003Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3107C>T
  hgvsp: ENSP00000474748.1:p.Ala1036Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.931C>T
  hgvsp: ENSP00000415612.1:p.Ala311Val
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13506
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1041Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

10-75556645-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556645
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556645
    reference: chr 10
allele count: 4
allele frequency: 3.314880498558027e-5
allele num: 120668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.949C>T
  hgvsp: ENST00000604754.1:c.949C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1989C>T
  hgvsp: ENST00000492395.1:c.1989C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3126C>T
  hgvsp: ENST00000433366.2:c.3126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3033C>T
  hgvsp: ENST00000603114.1:c.3033C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3147C>T
  hgvsp: ENST00000398706.2:c.3147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3147C>T
  hgvsp: ENST00000604729.1:c.3147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3132C>T
  hgvsp: ENST00000605216.1:c.3132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1150C>T
  hgvsp: ENST00000603187.1:c.1150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3132C>T
  hgvsp: ENST00000604524.1:c.3132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.147C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.956C>T
  hgvsp: ENST00000412198.1:c.956C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1087G>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2373G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His1049His
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-75556646-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556646
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556646
    reference: chr 10
allele count: 7
allele frequency: 5.801521656251554e-5
allele num: 120658
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2372C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3148G>A
  hgvsp: ENSP00000474944.1:p.Gly1050Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1151G>A
  hgvsp: ENSP00000474766.1:p.Gly385Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3133G>A
  hgvsp: ENSP00000474748.1:p.Gly1045Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.148G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3133G>A
  hgvsp: ENSP00000474348.1:p.Gly1045Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1086C>T
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3127G>A
  hgvsp: ENSP00000387828.2:p.Gly1043Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1990G>A
  hgvsp: ENSP00000432423.1:p.Gly664Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3148G>A
  hgvsp: ENSP00000381693.2:p.Gly1050Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3034G>A
  hgvsp: ENSP00000474043.1:p.Gly1012Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.957G>A
  hgvsp: ENSP00000415612.1:p.Gly320Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.950G>A
  hgvsp: ENSP00000474118.1:p.Gly318Arg
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly1050Arg
num of homozygotes: 1
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-75556655-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556655
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556655
    reference: chr 10
allele count: 1
allele frequency: 8.294074713025015e-6
allele num: 120568
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.1999T>C
  hgvsp: ENSP00000432423.1:p.Ser667Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3142T>C
  hgvsp: ENSP00000474748.1:p.Ser1048Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3157T>C
  hgvsp: ENSP00000474944.1:p.Ser1053Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1160T>C
  hgvsp: ENSP00000474766.1:p.Ser388Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.966T>C
  hgvsp: ENSP00000415612.1:p.Ser323Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3157T>C
  hgvsp: ENSP00000381693.2:p.Ser1053Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1077A>G
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.157T>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3043T>C
  hgvsp: ENSP00000474043.1:p.Ser1015Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3142T>C
  hgvsp: ENSP00000474348.1:p.Ser1048Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3136T>C
  hgvsp: ENSP00000387828.2:p.Ser1046Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.959T>C
  hgvsp: ENSP00000474118.1:p.Ser321Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2363A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1053Pro
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

10-75556658-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556658
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556658
    reference: chr 10
allele count: 1
allele frequency: 8.297240337863626e-6
allele num: 120522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1163G>A
  hgvsp: ENSP00000474766.1:p.Ala389Thr
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3046G>A
  hgvsp: ENSP00000474043.1:p.Ala1016Thr
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1074C>T
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3139G>A
  hgvsp: ENSP00000387828.2:p.Ala1047Thr
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3145G>A
  hgvsp: ENSP00000474348.1:p.Ala1049Thr
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.962G>A
  hgvsp: ENSP00000474118.1:p.Ala322Thr
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2002G>A
  hgvsp: ENSP00000432423.1:p.Ala668Thr
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3145G>A
  hgvsp: ENSP00000474748.1:p.Ala1049Thr
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3160G>A
  hgvsp: ENSP00000381693.2:p.Ala1054Thr
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2360C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.969G>A
  hgvsp: ENSP00000415612.1:p.Ala324Thr
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.160G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3160G>A
  hgvsp: ENSP00000474944.1:p.Ala1054Thr
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13457
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1054Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

10-75556660-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556660
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556660
    reference: chr 10
allele count: 2
allele frequency: 1.659227795384028e-5
allele num: 120538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3162C>T
  hgvsp: ENST00000604729.1:c.3162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3162C>T
  hgvsp: ENST00000398706.2:c.3162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.971C>T
  hgvsp: ENST00000412198.1:c.971C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2358G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2004C>T
  hgvsp: ENST00000492395.1:c.2004C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3048C>T
  hgvsp: ENST00000603114.1:c.3048C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3147C>T
  hgvsp: ENST00000604524.1:c.3147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1165C>T
  hgvsp: ENST00000603187.1:c.1165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3141C>T
  hgvsp: ENST00000433366.2:c.3141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.162C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3147C>T
  hgvsp: ENST00000605216.1:c.3147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1072G>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.964C>T
  hgvsp: ENST00000604754.1:c.964C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1054Ala
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

10-75556662-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556662
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556662
    reference: chr 10
allele count: 1
allele frequency: 8.29737802854298e-6
allele num: 120520
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3149C>T
  hgvsp: ENSP00000474748.1:p.Pro1050Leu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1167C>T
  hgvsp: ENSP00000474766.1:p.Pro390Leu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2006C>T
  hgvsp: ENSP00000432423.1:p.Pro669Leu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2356G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3164C>T
  hgvsp: ENSP00000474944.1:p.Pro1055Leu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3164C>T
  hgvsp: ENSP00000381693.2:p.Pro1055Leu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3149C>T
  hgvsp: ENSP00000474348.1:p.Pro1050Leu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.973C>T
  hgvsp: ENSP00000415612.1:p.Pro325Leu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.164C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3143C>T
  hgvsp: ENSP00000387828.2:p.Pro1048Leu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.966C>T
  hgvsp: ENSP00000474118.1:p.Pro323Leu
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1070G>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3050C>T
  hgvsp: ENSP00000474043.1:p.Pro1017Leu
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1055Leu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS

10-75556674-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556674
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556674
    reference: chr 10
allele count: 1
allele frequency: 8.306613725848521e-6
allele num: 120386
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1058T>C
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3161A>G
  hgvsp: ENSP00000474348.1:p.Gln1054Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3161A>G
  hgvsp: ENSP00000474748.1:p.Gln1054Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2344T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.176A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3176A>G
  hgvsp: ENSP00000474944.1:p.Gln1059Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2018A>G
  hgvsp: ENSP00000432423.1:p.Gln673Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3155A>G
  hgvsp: ENSP00000387828.2:p.Gln1052Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1179A>G
  hgvsp: ENSP00000474766.1:p.Gln394Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.978A>G
  hgvsp: ENSP00000474118.1:p.Gln327Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3062A>G
  hgvsp: ENSP00000474043.1:p.Gln1021Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.985A>G
  hgvsp: ENSP00000415612.1:p.Gln329Arg
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3176A>G
  hgvsp: ENSP00000381693.2:p.Gln1059Arg
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1059Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

10-75556675-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556675
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556675
    reference: chr 10
allele count: 1
allele frequency: 8.30813199960121e-6
allele num: 120364
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1057T>C
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2343T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.979A>G
  hgvsp: ENST00000604754.1:c.979A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2019A>G
  hgvsp: ENST00000492395.1:c.2019A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.177A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3177A>G
  hgvsp: ENST00000398706.2:c.3177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1180A>G
  hgvsp: ENST00000603187.1:c.1180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.986A>G
  hgvsp: ENST00000412198.1:c.986A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3162A>G
  hgvsp: ENST00000604524.1:c.3162A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3156A>G
  hgvsp: ENST00000433366.2:c.3156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3063A>G
  hgvsp: ENST00000603114.1:c.3063A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3177A>G
  hgvsp: ENST00000604729.1:c.3177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3162A>G
  hgvsp: ENST00000605216.1:c.3162A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1059Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

10-75556681-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556681
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556681
    reference: chr 10
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2025G>C
  hgvsp: ENST00000492395.1:c.2025G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1051C>G
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1186G>C
  hgvsp: ENST00000603187.1:c.1186G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3183G>C
  hgvsp: ENST00000604729.1:c.3183G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.985G>C
  hgvsp: ENST00000604754.1:c.985G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3168G>C
  hgvsp: ENST00000605216.1:c.3168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3162G>C
  hgvsp: ENST00000433366.2:c.3162G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3168G>C
  hgvsp: ENST00000604524.1:c.3168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3183G>C
  hgvsp: ENST00000398706.2:c.3183G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.992G>C
  hgvsp: ENST00000412198.1:c.992G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.183G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2337C>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3069G>C
  hgvsp: ENST00000603114.1:c.3069G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1061Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

10-75556703-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556703
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556703
    reference: chr 10
allele count: 1
allele frequency: 8.344041519950603e-6
allele num: 119846
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2047G>C
  hgvsp: ENSP00000432423.1:p.Ala683Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3190G>C
  hgvsp: ENSP00000474348.1:p.Ala1064Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.1007G>C
  hgvsp: ENSP00000474118.1:p.Ala337Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1208G>C
  hgvsp: ENSP00000474766.1:p.Ala404Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3205G>C
  hgvsp: ENSP00000474944.1:p.Ala1069Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1029C>G
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3184G>C
  hgvsp: ENSP00000387828.2:p.Ala1062Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.205G>C
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3091G>C
  hgvsp: ENSP00000474043.1:p.Ala1031Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3205G>C
  hgvsp: ENSP00000381693.2:p.Ala1069Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.1014G>C
  hgvsp: ENSP00000415612.1:p.Ala339Pro
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2315C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3190G>C
  hgvsp: ENSP00000474748.1:p.Ala1064Pro
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1069Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

10-75556704-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556704
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556704
    reference: chr 10
allele count: 1
allele frequency: 8.343623802689983e-6
allele num: 119852
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1028G>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3206C>T
  hgvsp: ENSP00000474944.1:p.Ala1069Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3191C>T
  hgvsp: ENSP00000474348.1:p.Ala1064Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.1008C>T
  hgvsp: ENSP00000474118.1:p.Ala337Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3185C>T
  hgvsp: ENSP00000387828.2:p.Ala1062Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2048C>T
  hgvsp: ENSP00000432423.1:p.Ala683Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3092C>T
  hgvsp: ENSP00000474043.1:p.Ala1031Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3191C>T
  hgvsp: ENSP00000474748.1:p.Ala1064Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3206C>T
  hgvsp: ENSP00000381693.2:p.Ala1069Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1209C>T
  hgvsp: ENSP00000474766.1:p.Ala404Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.206C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.1015C>T
  hgvsp: ENSP00000415612.1:p.Ala339Val
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2314G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1069Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

10-75556708-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556708
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556708
    reference: chr 10
allele count: 1
allele frequency: 8.347663488989432e-6
allele num: 119794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.1019A>G
  hgvsp: ENST00000412198.1:c.1019A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1024T>C
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3210A>G
  hgvsp: ENST00000398706.2:c.3210A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.210A>G
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3210A>G
  hgvsp: ENST00000604729.1:c.3210A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2310T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2052A>G
  hgvsp: ENST00000492395.1:c.2052A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3195A>G
  hgvsp: ENST00000604524.1:c.3195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3189A>G
  hgvsp: ENST00000433366.2:c.3189A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1213A>G
  hgvsp: ENST00000603187.1:c.1213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3096A>G
  hgvsp: ENST00000603114.1:c.3096A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.1012A>G
  hgvsp: ENST00000604754.1:c.1012A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3195A>G
  hgvsp: ENST00000605216.1:c.3195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1070Gln
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

10-75556714-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556714
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556714
    reference: chr 10
allele count: 17
allele frequency: 1.421404682274248e-4
allele num: 119600
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.1018C>T
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3216G>A
  hgvsp: ENST00000398706.2:c.3216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3201G>A
  hgvsp: ENST00000605216.1:c.3201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3195G>A
  hgvsp: ENST00000433366.2:c.3195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.1018G>A
  hgvsp: ENST00000604754.1:c.1018G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3102G>A
  hgvsp: ENST00000603114.1:c.3102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2304C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1219G>A
  hgvsp: ENST00000603187.1:c.1219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2058G>A
  hgvsp: ENST00000492395.1:c.2058G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3216G>A
  hgvsp: ENST00000604729.1:c.3216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.1025G>A
  hgvsp: ENST00000412198.1:c.1025G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.216G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3201G>A
  hgvsp: ENST00000604524.1:c.3201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly1072Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

10-75556739-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556739
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556739
    reference: chr 10
allele count: 3
allele frequency: 2.526613663926695e-5
allele num: 118736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.241C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3127C>T
  hgvsp: ENSP00000474043.1:p.Pro1043Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3241C>T
  hgvsp: ENSP00000474944.1:p.Pro1081Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.1050C>T
  hgvsp: ENSP00000415612.1:p.Pro351Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3226C>T
  hgvsp: ENSP00000474348.1:p.Pro1076Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2083C>T
  hgvsp: ENSP00000432423.1:p.Pro695Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.1043C>T
  hgvsp: ENSP00000474118.1:p.Pro349Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2279G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3226C>T
  hgvsp: ENSP00000474748.1:p.Pro1076Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3220C>T
  hgvsp: ENSP00000387828.2:p.Pro1074Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1244C>T
  hgvsp: ENSP00000474766.1:p.Pro416Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3241C>T
  hgvsp: ENSP00000381693.2:p.Pro1081Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.993G>A
  variant of: http://identifiers.org/hgnc/45103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1081Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

10-75556748-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556748
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556748
    reference: chr 10
allele count: 2
allele frequency: 1.6875073828448e-5
allele num: 118518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3250G>A
  hgvsp: ENSP00000474944.1:p.Gly1084Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2092G>A
  hgvsp: ENSP00000432423.1:p.Gly698Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3235G>A
  hgvsp: ENSP00000474348.1:p.Gly1079Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2270C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.984C>T
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3136G>A
  hgvsp: ENSP00000474043.1:p.Gly1046Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1253G>A
  hgvsp: ENSP00000474766.1:p.Gly419Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3250G>A
  hgvsp: ENSP00000381693.2:p.Gly1084Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.250G>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.1052G>A
  hgvsp: ENSP00000474118.1:p.Gly352Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3229G>A
  hgvsp: ENSP00000387828.2:p.Gly1077Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.1059G>A
  hgvsp: ENSP00000415612.1:p.Gly354Ser
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3235G>A
  hgvsp: ENSP00000474748.1:p.Gly1079Ser
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12435
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly1084Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

10-75556750-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556750
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556750
    reference: chr 10
allele count: 9
allele frequency: 7.595834106983104e-5
allele num: 118486
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3237C>T
  hgvsp: ENST00000604524.1:c.3237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.1061C>T
  hgvsp: ENST00000412198.1:c.1061C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2268G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.252C>T
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3252C>T
  hgvsp: ENST00000398706.2:c.3252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3231C>T
  hgvsp: ENST00000433366.2:c.3231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3237C>T
  hgvsp: ENST00000605216.1:c.3237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2094C>T
  hgvsp: ENST00000492395.1:c.2094C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.1054C>T
  hgvsp: ENST00000604754.1:c.1054C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.982G>A
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1255C>T
  hgvsp: ENST00000603187.1:c.1255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3252C>T
  hgvsp: ENST00000604729.1:c.3252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3138C>T
  hgvsp: ENST00000603114.1:c.3138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly1084Gly
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

10-75556751-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75556751
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 75556751
    reference: chr 10
allele count: 13
allele frequency: 1.096805764136139e-4
allele num: 118526
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000381693
  ensembl transcript: ENST00000398706
  gene symbol: ZSWIM8
  hgvsc: ENST00000398706.2:c.3253T>A
  hgvsp: ENSP00000381693.2:p.Phe1085Ile
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000387828
  ensembl transcript: ENST00000433366
  gene symbol: ZSWIM8
  hgvsc: ENST00000433366.2:c.3232T>A
  hgvsp: ENSP00000387828.2:p.Phe1078Ile
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474766
  ensembl transcript: ENST00000603187
  gene symbol: ZSWIM8
  hgvsc: ENST00000603187.1:c.1256T>A
  hgvsp: ENSP00000474766.1:p.Phe420Ile
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474118
  ensembl transcript: ENST00000604754
  gene symbol: ZSWIM8
  hgvsc: ENST00000604754.1:c.1055T>A
  hgvsp: ENSP00000474118.1:p.Phe353Ile
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000415612
  ensembl transcript: ENST00000412198
  gene symbol: ZSWIM8
  hgvsc: ENST00000412198.1:c.1062T>A
  hgvsp: ENSP00000415612.1:p.Phe355Ile
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214655
  ensembl transcript: ENST00000487278
  gene symbol: ZSWIM8
  hgvsc: ENST00000487278.1:n.253T>A
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000432423
  ensembl transcript: ENST00000492395
  gene symbol: ZSWIM8
  hgvsc: ENST00000492395.1:c.2095T>A
  hgvsp: ENSP00000432423.1:p.Phe699Ile
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272589
  ensembl transcript: ENST00000456638
  gene symbol: ZSWIM8-AS1
  hgvsc: ENST00000456638.2:n.981A>T
  variant of: http://identifiers.org/hgnc/45103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474043
  ensembl transcript: ENST00000603114
  gene symbol: ZSWIM8
  hgvsc: ENST00000603114.1:c.3139T>A
  hgvsp: ENSP00000474043.1:p.Phe1047Ile
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474944
  ensembl transcript: ENST00000604729
  gene symbol: ZSWIM8
  hgvsc: ENST00000604729.1:c.3253T>A
  hgvsp: ENSP00000474944.1:p.Phe1085Ile
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474748
  ensembl transcript: ENST00000605216
  gene symbol: ZSWIM8
  hgvsc: ENST00000605216.1:c.3238T>A
  hgvsp: ENSP00000474748.1:p.Phe1080Ile
  variant of: http://identifiers.org/hgnc/23528
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272916
  ensembl protein: ENSP00000475031
  ensembl transcript: ENST00000603027
  gene symbol: RP11-574K11.31
  hgvsc: ENST00000603027.1:c.*2267A>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214655
  ensembl protein: ENSP00000474348
  ensembl transcript: ENST00000604524
  gene symbol: ZSWIM8
  hgvsc: ENST00000604524.1:c.3238T>A
  hgvsp: ENSP00000474348.1:p.Phe1080Ile
  variant of: http://identifiers.org/hgnc/23528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe1085Ile
num of homozygotes: 1
reference allele: T

GenotypeDepth
all individuals: 267
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 216
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2500
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42010
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 124
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1008
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2077
bin: 7.75e1
variant carriers: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

African
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allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
num of homozygotes: 0

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

InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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SIO_000300: 5.981e1

BaseQRankSum
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SIO_000300: -2.695e0

ClippingRankSum
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SIO_000300: 6.66e-1

QD
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FS
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ReadPosRankSum
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SIO_000300: -5.95e-1

DP
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SIO_000300: 1.761607e6

GenotypeDepth
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variant carriers: 3

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66522
num of homozygotes: 0

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

African
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allele count: 4
allele frequency: 4.099200655872105e-4
allele num: 9758
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.75834e6

ReadPosRankSum
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SIO_000300: -2.07e-1

MQ
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FS
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VQSLOD
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ClippingRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 5.0e-4

MQRankSum
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SIO_000300: 1.07e0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503397678753984e-5
allele num: 66516
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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FS
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MQ
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VQSLOD
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BaseQRankSum
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SIO_000300: 7.38e-1

ClippingRankSum
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SIO_000300: -9.350000000000001e-1

QD
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SIO_000300: 5.16e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

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

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

East Asian
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allele count: 4
allele frequency: 4.697040864255519e-4
allele num: 8516
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.822821728034998e-4
allele num: 16458
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.537342327354124e-5
allele num: 66118
num of homozygotes: 0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.064e0

BaseQRankSum
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MQ
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SIO_000300: 5.97e1

ClippingRankSum
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SIO_000300: -2.91e-1

QD
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InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.739913e6

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 1
allele frequency: 1.176747469992939e-4
allele num: 8498
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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66064
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African
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Other
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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African
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 65922
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Other
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QD
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VQSLOD
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BaseQRankSum
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DP
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

East Asian
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Other
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African
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.837044892188053e-5
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65252
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MQ
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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European (Non-Finnish)
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Latino
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European (Finnish)
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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FS
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DP
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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QD
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MQRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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FS
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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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GenotypeQuality
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Latino
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allele frequency: 9.926543577526305e-5
allele num: 10074
num of homozygotes: 0

European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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African
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East Asian
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 60230
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 57878
num of homozygotes: 0

Latino
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allele frequency: 3.309066843150232e-4
allele num: 9066
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
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MQ
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SIO_000300: 6.0e1

MQRankSum
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InbreedingCoeff
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SIO_000300: -4.5e-3

QD
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DP
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 4.29e-1

ClippingRankSum
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SIO_000300: -3.4e-1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6216
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 8794
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57058
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African
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allele frequency: 3.533568904593639e-4
allele num: 8490
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Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 0.0e0

MQ
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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FS
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ClippingRankSum
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SIO_000300: 3.64e-1

VQSLOD
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DP
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SIO_000300: 1.132556e6

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 3
allele frequency: 3.550295857988166e-4
allele num: 8450
num of homozygotes: 0

European (Non-Finnish)
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allele count: 13
allele frequency: 2.287363198085653e-4
allele num: 56834
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14988
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.147052076164258e-4
allele num: 8718
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East Asian
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: 2.46e-1

InbreedingCoeff
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MQ
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DP
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QD
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MQRankSum
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: -1.24e-1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
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InbreedingCoeff
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SIO_000300: -6.900000000000001e-2

FS
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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DP
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MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 1.063e1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
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Latino
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: NaN
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African
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allele count: 0
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South Asian
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ClippingRankSum
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FS
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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allele frequency: 2.768549280177187e-4
allele num: 3612
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European (Finnish)
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allele count: 0
allele frequency: NaN
allele num: 0
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Other
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allele count: 0
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FS
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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MQRankSum
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VQSLOD
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DP
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 22

African
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allele frequency: 1.170212765957447e-1
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South Asian
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allele frequency: 1.701208981001727e-1
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East Asian
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allele frequency: 1.333333333333333e-1
allele num: 90
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European (Finnish)
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allele frequency: NaN
allele num: 0
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Other
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allele frequency: 2.307692307692308e-1
allele num: 26
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European (Non-Finnish)
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Latino
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ClippingRankSum
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DP
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MQ
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MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

South Asian
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allele count: 115
allele frequency: 4.96545768566494e-2
allele num: 2316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 5.0e-2
allele num: 940
num of homozygotes: 0

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

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

East Asian
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allele count: 0
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num of homozygotes: 0

Latino
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Other
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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ClippingRankSum
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MQ
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DP
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: -4.09e-2

GenotypeQuality
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variant carriers: 1

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

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

European (Finnish)
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allele frequency: NaN
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num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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FS
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SIO_000300: 0.0e0

MQ
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InbreedingCoeff
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VQSLOD
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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Other
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African
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Latino
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South Asian
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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African
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European (Finnish)
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DP
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MQRankSum
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FS
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VQSLOD
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MQ
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QD
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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Other
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European (Finnish)
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East Asian
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Latino
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DP
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ClippingRankSum
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QD
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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MQ
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MQRankSum
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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VQSLOD
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BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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FS
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60748
num of homozygotes: 0

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

European (Finnish)
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European (Non-Finnish)
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Other
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Latino
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East Asian
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African
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DP
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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VQSLOD
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QD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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FS
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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African
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Other
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
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QD
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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African
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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BaseQRankSum
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ClippingRankSum
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QD
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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SIO_000300: 6.0e-2

FS
type: SiteQuality
SIO_000300: 5.669e0

MQ
type: SiteQuality
SIO_000300: 5.633e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.25e1
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
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.158659464923087e-5
allele num: 63318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7948
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9080
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10876
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

MQRankSum
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SIO_000300: 5.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 4.787e0

ReadPosRankSum
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SIO_000300: 6.39e-1

QD
type: SiteQuality
SIO_000300: 1.308e1

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

DP
type: SiteQuality
SIO_000300: 1.341092e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 2.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16146
num of homozygotes: 0

Other
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: 11088
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.555209953343701e-5
allele num: 64300
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8104
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.369942e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.598e1

BaseQRankSum
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SIO_000300: -3.575e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

FS
type: SiteQuality
SIO_000300: 2.764e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16206
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11190
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64658
num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.135383301302584e-4
allele num: 9366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -4.625e0

QD
type: SiteQuality
SIO_000300: 1.482e1

VQSLOD
type: SiteQuality
SIO_000300: 3.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.006e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.378591e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531675039823551e-5
allele num: 65288
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

South Asian
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
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

VQSLOD
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DP
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MQ
type: SiteQuality
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MQRankSum
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BaseQRankSum
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SIO_000300: -1.645e0

InbreedingCoeff
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SIO_000300: 1.5e-3

QD
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SIO_000300: 1.108e1

ReadPosRankSum
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SIO_000300: 1.07e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9614
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.187930624851509e-4
allele num: 8418
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

MQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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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: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
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 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: 8464
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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.027184113337773e-5
allele num: 66068
num of homozygotes: 0

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

GenotypeDepth
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.355712603062426e-4
allele num: 8490
num of homozygotes: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

Other
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num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 1.02124183006536e-4
allele num: 9792
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.500720115218435e-5
allele num: 66656
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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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 frequency: 0.0e0
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BaseQRankSum
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QD
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MQRankSum
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FS
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VQSLOD
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DP
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MQ
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 1

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

Latino
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allele count: 3
allele frequency: 2.592016588906169e-4
allele num: 11574
num of homozygotes: 0

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

MQ
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SIO_000300: 5.953e1

InbreedingCoeff
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BaseQRankSum
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MQRankSum
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VQSLOD
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DP
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QD
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FS
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SIO_000300: 5.38e-1

ReadPosRankSum
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SIO_000300: 4.09e-1

ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66588
num of homozygotes: 0

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502674761074713e-5
allele num: 66548
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

Latino
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allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

Other
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele num: 66564
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QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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FS
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 1
allele frequency: 1.024590163934426e-4
allele num: 9760
num of homozygotes: 0

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

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

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

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

Latino
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num of homozygotes: 0

South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66416
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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African
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allele num: 9714
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East Asian
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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VQSLOD
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BaseQRankSum
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MQ
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FS
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
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allele num: 66094
num of homozygotes: 0

Latino
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East Asian
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European (Finnish)
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South Asian
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Other
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African
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QD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 9582
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South Asian
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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East Asian
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FS
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Latino
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European (Non-Finnish)
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South Asian
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European (Finnish)
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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DP
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MQ
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 4

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46607
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 9.75e1
variant carriers: 17

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

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.213187346455976e-4
allele num: 65942
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.463154060944518e-4
allele num: 16474
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.536e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.405229e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.06e0

QD
type: SiteQuality
SIO_000300: 1.344e1

GenotypeDepth
all individuals: 170
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 1

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

GenotypeDepth
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44901
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 3.203759077317386e-4
allele num: 9364
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65420
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
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: 2.739e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.7e-2

MQ
type: SiteQuality
SIO_000300: 5.954e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

DP
type: SiteQuality
SIO_000300: 1.387743e6

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 779
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 1558
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variant carriers: 0

GenotypeQuality
all individuals: 5752
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
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GenotypeQuality
all individuals: 205
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variant carriers: 0

GenotypeQuality
all individuals: 44500
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 656
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16240
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.734906315058987e-4
allele num: 11528
num of homozygotes: 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: 884
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 1.382281e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
SIO_000300: 1.432e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.06e-1

GenotypeDepth
all individuals: 238
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 39738
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variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 158
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variant carriers: 0

GenotypeQuality
all individuals: 44346
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1752
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variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 295
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variant carriers: 0

GenotypeQuality
all individuals: 1558
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variant carriers: 0

GenotypeQuality
all individuals: 5728
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
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GenotypeQuality
all individuals: 775
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variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
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GenotypeQuality
all individuals: 1979
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GenotypeQuality
all individuals: 628
bin: 9.75e1
variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 669
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GenotypeQuality
all individuals: 195
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.063256241384592e-5
allele num: 65290
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.642525533890436e-4
allele num: 8616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.515610791148833e-4
allele num: 6598
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.233045622688039e-4
allele num: 16220
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.261e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 5.37e0

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.381453e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

QD
type: SiteQuality
SIO_000300: 1.318e1