11-1857312-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857312
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857312
    reference: chr 11
allele count: 1
allele frequency: 1.90759604746099e-5
allele num: 52422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1277A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.911A>T
  hgvsp: ENSP00000443325.1:p.Asp304Val
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.593A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.54A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-44A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.254A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.455A>T
  hgvsp: ENSP00000414626.2:p.Asp152Val
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-44A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000475245
  gene symbol: SYT8
  hgvsc: ENST00000475245.1:n.497A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2291A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.775A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-44A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-44A>T
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24593
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19917
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp304Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

11-1857317-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857317
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857317
    reference: chr 11
allele count: 1
allele frequency: 2.093364036005861e-5
allele num: 47770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.59G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.259G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2296G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.780G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.916G>A
  hgvsp: ENSP00000443325.1:p.Ala306Thr
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1282G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000475245
  gene symbol: SYT8
  hgvsc: ENST00000475245.1:n.502G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.460G>A
  hgvsp: ENSP00000414626.2:p.Ala154Thr
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-39G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-39G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.598G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-39G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-39G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25228
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9830
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18920
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala306Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-1857321-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857321
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857321
    reference: chr 11
allele count: 1
allele frequency: 2.296633135822884e-5
allele num: 43542
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-35G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.263G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.784G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-35G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-35G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2300G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.464G>T
  hgvsp: ENSP00000414626.2:p.Gly155Val
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.920G>T
  hgvsp: ENSP00000443325.1:p.Gly307Val
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.602G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-35G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.63G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000475245
  gene symbol: SYT8
  hgvsc: ENST00000475245.1:n.506G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1286G>T
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25917
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly307Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

11-1857325-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857325
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857325
    reference: chr 11
allele count: 2
allele frequency: 5.072537283149031e-5
allele num: 39428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2304C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.267C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.67C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.606C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000475245
  gene symbol: SYT8
  hgvsc: ENST00000475245.1:n.510C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1290C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.924C>T
  hgvsp: ENST00000535046.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.468C>T
  hgvsp: ENST00000436964.2:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-31C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.788C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-31C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-31C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-31C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16168
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala308Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/11-1857326-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857326
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857326
    reference: chr 11
allele count: 13
allele frequency: 3.435699561287594e-4
allele num: 37838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.607C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000475245
  gene symbol: SYT8
  hgvsc: ENST00000475245.1:n.511C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.268C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2305C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.789C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.925C>A
  hgvsp: ENSP00000443325.1:p.Leu309Ile
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-30C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.68C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-30C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1291C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-30C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-30C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.469C>A
  hgvsp: ENSP00000414626.2:p.Leu157Ile
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26715
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15649
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12773
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu309Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

11-1857328-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857328
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857328
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 37404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-28T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.609T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2307T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.270T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.70T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000475245
  gene symbol: SYT8
  hgvsc: ENST00000475245.1:n.513T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-28T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1293T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.927T>C
  hgvsp: ENST00000535046.1:c.927T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-28T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.471T>C
  hgvsp: ENST00000436964.2:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.791T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-28T>C
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27002
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13020
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu309Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

11-1857338-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857338
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857338
    reference: chr 11
allele count: 1
allele frequency: 3.442103813851025e-5
allele num: 29052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*4C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1303C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-18C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.280C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.80C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-18C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2317C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.619C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-18C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.801C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-18C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

11-1857340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857340
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857340
    reference: chr 11
allele count: 337
allele frequency: 1.198605776070565e-2
allele num: 28116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.282C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.803C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-16C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.621C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-16C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*6C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*6C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.82C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1305C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2319C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-16C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-16C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15757
  bin: 2.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 2.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 1.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 28441
  bin: 7.5e0
  variant carriers: 308
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11414
  bin: 1.25e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 14
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

11-1857341-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857341
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857341
    reference: chr 11
allele count: 1
allele frequency: 3.850596842510589e-5
allele num: 25970
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.283C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.83C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.622C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-15C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2320C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*7C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1306C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-15C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-15C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*7C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-15C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.804C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28695
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

11-1857343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857343
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857343
    reference: chr 11
allele count: 11
allele frequency: 4.25071489295927e-4
allele num: 25878
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*9C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-13C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.285C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.624C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-13C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.806C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.85C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-13C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*9C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2322C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-13C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1308C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16305
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10506
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 28957
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

11-1857344-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857344
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857344
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 25732
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-12G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2323G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*10G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-12G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-12G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.625G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-12G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*10G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.286G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.807G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.86G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1309G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29177
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

11-1857355-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857355
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857355
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 24450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*21G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.97G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*21G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395-1G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2334G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358-1G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400-1G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.297G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.636G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375-1G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1320G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.818G>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: splice acceptor
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29593
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17035
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.400-1G>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-1857356-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857356
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857356
    reference: chr 11
allele count: 4
allele frequency: 1.628797133317045e-4
allele num: 24558
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1321A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395A>C
  hgvsp: ENSP00000371406.3:p.Ile133Leu
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*22A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.298A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400A>C
  hgvsp: ENSP00000371394.3:p.Ile134Leu
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*22A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375A>C
  hgvsp: ENSP00000405850.1:p.Arg125Ser
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.637A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358A>C
  hgvsp: ENSP00000343691.3:p.Ile120Leu
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2335A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.819A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.98A>C
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17004
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile134Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

11-1857356-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857356
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857356
    reference: chr 11
allele count: 1
allele frequency: 4.071992833292614e-5
allele num: 24558
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.98A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*22A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.298A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400A>G
  hgvsp: ENSP00000371394.3:p.Ile134Val
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1321A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.637A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395A>G
  hgvsp: ENSP00000371406.3:p.Ile133Val
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2335A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.819A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375A>G
  hgvsp: ENST00000424556.2:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*22A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358A>G
  hgvsp: ENSP00000343691.3:p.Ile120Val
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17004
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile134Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-1857356-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857356
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857356
    reference: chr 11
allele count: 1
allele frequency: 4.071992833292614e-5
allele num: 24558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.819A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2335A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*22A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*22A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.395A>T
  hgvsp: ENSP00000371406.3:p.Ile133Phe
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1321A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.298A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.375A>T
  hgvsp: ENSP00000405850.1:p.Arg125Ser
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.358A>T
  hgvsp: ENSP00000343691.3:p.Ile120Phe
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.400A>T
  hgvsp: ENSP00000371394.3:p.Ile134Phe
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.637A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.98A>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17004
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile134Phe
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-1857360-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857360
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857360
    reference: chr 11
allele count: 1
allele frequency: 4.122011541632317e-5
allele num: 24260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.399G>A
  hgvsp: ENSP00000371406.3:p.Arg134Lys
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.404G>A
  hgvsp: ENSP00000371394.3:p.Arg135Lys
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1325G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.379G>A
  hgvsp: ENSP00000405850.1:p.Gly127Arg
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.641G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2339G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*26G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*26G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.102G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.362G>A
  hgvsp: ENSP00000343691.3:p.Arg121Lys
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.823G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.302G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg135Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-1857361-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857361
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857361
    reference: chr 11
allele count: 1
allele frequency: 4.098360655737705e-5
allele num: 24400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.303G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*27G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.405G>A
  hgvsp: ENST00000381968.3:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.400G>A
  hgvsp: ENST00000381978.3:c.400G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.103G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.642G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.380G>A
  hgvsp: ENSP00000405850.1:p.Gly127Glu
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1326G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2340G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*27G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.363G>A
  hgvsp: ENST00000341958.3:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.824G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9087
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29663
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly127Glu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-1857362-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857362
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857362
    reference: chr 11
allele count: 1
allele frequency: 4.129501156260323e-5
allele num: 24216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.401G>A
  hgvsp: ENSP00000371406.3:p.Val135Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.381G>A
  hgvsp: ENST00000424556.2:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.104G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.364G>A
  hgvsp: ENSP00000343691.3:p.Val122Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.406G>A
  hgvsp: ENSP00000371394.3:p.Val136Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.643G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*28G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*28G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1327G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.825G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2341G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.304G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9018
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val136Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

11-1857364-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857364
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857364
    reference: chr 11
allele count: 5
allele frequency: 2.062706270627063e-4
allele num: 24240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.383G>A
  hgvsp: ENSP00000405850.1:p.Trp128Ter
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*30G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*30G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2343G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.403G>A
  hgvsp: ENST00000381978.3:c.403G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.106G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.366G>A
  hgvsp: ENST00000341958.3:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.645G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.408G>A
  hgvsp: ENST00000381968.3:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.306G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.827G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1329G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8969
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29695
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp128Ter
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

11-1857378-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857378
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857378
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 23386
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.422C>T
  hgvsp: ENSP00000371394.3:p.Ala141Val
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.120C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*44C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.380C>T
  hgvsp: ENSP00000343691.3:p.Ala127Val
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*44C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*7C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2357C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.659C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.417C>T
  hgvsp: ENSP00000371406.3:p.Ala140Val
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.841C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1343C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.320C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16721
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30515
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala141Val
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/11-1857381-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857381
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857381
    reference: chr 11
allele count: 2
allele frequency: 8.526603001364257e-5
allele num: 23456
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.425C>A
  hgvsp: ENSP00000371394.3:p.Ala142Asp
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.662C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.383C>A
  hgvsp: ENSP00000343691.3:p.Ala128Asp
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*47C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1346C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.323C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2360C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*10C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.420C>A
  hgvsp: ENSP00000371406.3:p.Ala141Asp
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.844C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*47C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.123C>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8242
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30939
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala142Asp
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

11-1857383-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857383
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857383
    reference: chr 11
allele count: 1
allele frequency: 4.151444702756559e-5
allele num: 24088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*49G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.427G>A
  hgvsp: ENSP00000371394.3:p.Asp143Asn
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2362G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.125G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.422G>A
  hgvsp: ENSP00000371406.3:p.Asp142Asn
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.385G>A
  hgvsp: ENSP00000343691.3:p.Asp129Asn
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.846G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*12G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.664G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1348G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*49G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.325G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15750
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31464
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp143Asn
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

11-1857399-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857399
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857399
    reference: chr 11
allele count: 1
allele frequency: 3.595311713525563e-5
allele num: 27814
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.862G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*65G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.438G>A
  hgvsp: ENSP00000371406.3:p.Gly147Asp
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.341G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1364G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.443G>A
  hgvsp: ENSP00000371394.3:p.Gly148Asp
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*65G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*28G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.141G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2378G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.401G>A
  hgvsp: ENSP00000343691.3:p.Gly134Asp
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.680G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11498
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34252
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly148Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

11-1857403-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857403
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857403
    reference: chr 11
allele count: 1
allele frequency: 3.445661911653229e-5
allele num: 29022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*32C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.405C>T
  hgvsp: ENST00000341958.3:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.866C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.447C>T
  hgvsp: ENST00000381968.3:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.442C>T
  hgvsp: ENST00000381978.3:c.442C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.145C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.345C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1368C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.684C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*69C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2382C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*69C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35166
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr149Thr
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

11-1857404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857404
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857404
    reference: chr 11
allele count: 11
allele frequency: 3.720993166903457e-4
allele num: 29562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*70G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*70G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.448G>A
  hgvsp: ENSP00000371394.3:p.Val150Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.406G>A
  hgvsp: ENSP00000343691.3:p.Val136Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1369G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2383G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.146G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.443G>A
  hgvsp: ENSP00000371406.3:p.Val149Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.346G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.685G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.867G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*33G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35383
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val150Met
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-1857412-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857412
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857412
    reference: chr 11
allele count: 1
allele frequency: 2.999760019198464e-5
allele num: 33336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*78C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*41C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*78C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.456C>A
  hgvsp: ENST00000381968.3:c.456C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.451C>A
  hgvsp: ENST00000381978.3:c.451C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.693C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.875C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.414C>A
  hgvsp: ENST00000341958.3:c.414C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1377C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2391C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.154C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.354C>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35817
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro152Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

11-1857412-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857412
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857412
    reference: chr 11
allele count: 56
allele frequency: 1.67986561075114e-3
allele num: 33336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.693C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*78C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.451C>T
  hgvsp: ENST00000381978.3:c.451C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.875C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1377C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*41C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.456C>T
  hgvsp: ENST00000381968.3:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.154C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*78C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2391C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.354C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.414C>T
  hgvsp: ENST00000341958.3:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7290
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9024
  bin: 1.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 1.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 35817
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro152Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

11-1857419-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857419
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857419
    reference: chr 11
allele count: 3
allele frequency: 8.084510078689232e-5
allele num: 37108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.361C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*85C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.700C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.463C>T
  hgvsp: ENSP00000371394.3:p.Arg155Trp
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*85C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*48C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.458C>T
  hgvsp: ENSP00000371406.3:p.Arg154Trp
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.421C>T
  hgvsp: ENSP00000343691.3:p.Arg141Trp
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.882C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.161C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2398C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1384C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5813
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9085
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg155Trp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-1857420-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857420
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857420
    reference: chr 11
allele count: 3
allele frequency: 7.893490501499764e-5
allele num: 38006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1385G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.162G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.362G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*86G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.459G>A
  hgvsp: ENSP00000371406.3:p.Arg154Gln
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.464G>A
  hgvsp: ENSP00000371394.3:p.Arg155Gln
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.701G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2399G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*49G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.422G>A
  hgvsp: ENSP00000343691.3:p.Arg141Gln
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*86G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.883G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35185
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg155Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

11-1857421-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857421
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857421
    reference: chr 11
allele count: 8
allele frequency: 2.047082906857728e-4
allele num: 39080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.423G>A
  hgvsp: ENST00000341958.3:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2400G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.702G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1386G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.363G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*87G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*87G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.163G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*50G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.465G>A
  hgvsp: ENST00000381968.3:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.460G>A
  hgvsp: ENST00000381978.3:c.460G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.884G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8942
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg155Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

11-1857422-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857422
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857422
    reference: chr 11
allele count: 1
allele frequency: 2.523850386149109e-5
allele num: 39622
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.466G>A
  hgvsp: ENSP00000371394.3:p.Val156Ile
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.164G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.885G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.364G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.703G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*88G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*88G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.424G>A
  hgvsp: ENSP00000343691.3:p.Val142Ile
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2401G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*51G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1387G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.461G>A
  hgvsp: ENSP00000371406.3:p.Val155Ile
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8911
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34887
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val156Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

11-1857424-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857424
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857424
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 40680
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*53C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.366C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.463C>T
  hgvsp: ENST00000381978.3:c.463C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.468C>T
  hgvsp: ENST00000381968.3:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.705C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.426C>T
  hgvsp: ENST00000341958.3:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*90C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1389C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.166C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2403C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*90C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.887C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34588
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val156Val
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

11-1857426-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857426
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857426
    reference: chr 11
allele count: 3
allele frequency: 7.162639671473594e-5
allele num: 41884
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.470G>T
  hgvsp: ENSP00000371394.3:p.Ser157Ile
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.707G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*92G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.465G>T
  hgvsp: ENSP00000371406.3:p.Ser156Ile
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1391G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*92G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.428G>T
  hgvsp: ENSP00000343691.3:p.Ser143Ile
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*55G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.168G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.368G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2405G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.889G>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8451
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8799
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34333
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser157Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

11-1857427-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857427
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857427
    reference: chr 11
allele count: 18
allele frequency: 4.263382283278067e-4
allele num: 42220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*93C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.471C>T
  hgvsp: ENST00000381968.3:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.708C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.429C>T
  hgvsp: ENST00000341958.3:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.890C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*56C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1392C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*93C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2406C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.466C>T
  hgvsp: ENST00000381978.3:c.466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.169C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.369C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8807
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 34034
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4680
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser157Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

11-1857428-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857428
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857428
    reference: chr 11
allele count: 18
allele frequency: 4.115038178409767e-4
allele num: 43742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2407G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.891G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.472G>A
  hgvsp: ENSP00000371394.3:p.Val158Ile
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.467G>A
  hgvsp: ENSP00000371406.3:p.Val157Ile
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.709G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*94G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.370G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.170G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*57G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*94G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1393G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.430G>A
  hgvsp: ENSP00000343691.3:p.Val144Ile
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9519
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8630
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 33675
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val158Ile
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

11-1857434-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857434
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857434
    reference: chr 11
allele count: 35
allele frequency: 7.284685509719852e-4
allele num: 48046
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.436A>G
  hgvsp: ENSP00000343691.3:p.Thr146Ala
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2413A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.478A>G
  hgvsp: ENSP00000371394.3:p.Thr160Ala
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*100A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.176A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.376A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*63A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1399A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.473A>G
  hgvsp: ENSP00000371406.3:p.Thr159Ala
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.715A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*100A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.897A>G
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11855
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8307
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 32191
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr160Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

11-1857437-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857437
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857437
    reference: chr 11
allele count: 1
allele frequency: 1.985702938840349e-5
allele num: 50360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*103C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2416C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*103C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1402C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.439C>G
  hgvsp: ENSP00000343691.3:p.Gln147Glu
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.718C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.481C>G
  hgvsp: ENSP00000371394.3:p.Gln161Glu
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.476C>G
  hgvsp: ENSP00000371406.3:p.Gln160Glu
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.179C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*66C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.900C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.379C>G
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8035
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln161Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

11-1857442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857442
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857442
    reference: chr 11
allele count: 24
allele frequency: 4.406256884776382e-4
allele num: 54468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.184C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*71C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1407C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2421C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.481C>T
  hgvsp: ENST00000381978.3:c.481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.444C>T
  hgvsp: ENST00000341958.3:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.384C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*108C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*108C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.905C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.486C>T
  hgvsp: ENST00000381968.3:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.723C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29717
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 15351
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala162Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

11-1857443-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857443
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857443
    reference: chr 11
allele count: 1
allele frequency: 1.807599146813203e-5
allele num: 55322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*109G>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.385G>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.185G>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.482G>C
  hgvsp: ENSP00000371406.3:p.Gly162Arg
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1408G>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2422G>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.724G>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.906G>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.487G>C
  hgvsp: ENSP00000371394.3:p.Gly163Arg
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*109G>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.445G>C
  hgvsp: ENSP00000343691.3:p.Gly149Arg
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*72G>C
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly163Arg
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

11-1857445-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857445
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857445
    reference: chr 11
allele count: 1
allele frequency: 1.744165765514354e-5
allele num: 57334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*111A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*74A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.484A>T
  hgvsp: ENST00000381978.3:c.484A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.908A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.489A>T
  hgvsp: ENST00000381968.3:c.489A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.447A>T
  hgvsp: ENST00000341958.3:c.447A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.187A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.726A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*111A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1410A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2424A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.387A>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly163Gly
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

11-1857453-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857453
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857453
    reference: chr 11
allele count: 1
allele frequency: 1.638968105680664e-5
allele num: 61014
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.497A>G
  hgvsp: ENSP00000371394.3:p.His166Arg
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*82A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*119A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*119A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.734A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.916A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.492A>G
  hgvsp: ENSP00000371406.3:p.His165Arg
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.455A>G
  hgvsp: ENSP00000343691.3:p.His152Arg
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2432A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1418A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.195A>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.395A>G
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27084
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His166Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-1857460-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857460
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857460
    reference: chr 11
allele count: 2
allele frequency: 3.12236550410591e-5
allele num: 64054
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1425A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.499A>C
  hgvsp: ENST00000381978.3:c.499A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2439A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.504A>C
  hgvsp: ENST00000381968.3:c.504A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.462A>C
  hgvsp: ENST00000341958.3:c.462A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.741A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*126A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*89A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*126A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.202A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.402A>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.923A>C
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6670
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20065
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr168Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

11-1857465-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857465
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857465
    reference: chr 11
allele count: 2
allele frequency: 3.084896347482724e-5
allele num: 64832
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.509T>C
  hgvsp: ENSP00000371394.3:p.Val170Ala
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.407T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.504T>C
  hgvsp: ENSP00000371406.3:p.Val169Ala
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.467T>C
  hgvsp: ENSP00000343691.3:p.Val156Ala
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*131T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.746T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1430T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2444T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*131T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*94T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.207T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.928T>C
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25120
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val170Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

11-1857466-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857466
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857466
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 64574
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*132G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.505G>A
  hgvsp: ENST00000381978.3:c.505G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.468G>A
  hgvsp: ENST00000341958.3:c.468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*132G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.408G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*95G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.510G>A
  hgvsp: ENST00000381968.3:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1431G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.929G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2445G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.747G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.208G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25102
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val170Val
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

11-1857470-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857470
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857470
    reference: chr 11
allele count: 8
allele frequency: 1.226316757618493e-4
allele num: 65236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1435C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*99C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.509C>T
  hgvsp: ENSP00000371406.3:p.Arg171Ter
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*136C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.933C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.514C>T
  hgvsp: ENSP00000371394.3:p.Arg172Ter
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.412C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.472C>T
  hgvsp: ENSP00000343691.3:p.Arg158Ter
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.751C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2449C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*136C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.212C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24596
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19700
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7204
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg172Ter
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

11-1857471-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857471
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857471
    reference: chr 11
allele count: 13
allele frequency: 1.979896436186415e-4
allele num: 65660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1436G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.934G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.213G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.510G>A
  hgvsp: ENSP00000371406.3:p.Arg171Gln
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*137G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.515G>A
  hgvsp: ENSP00000371394.3:p.Arg172Gln
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*137G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.473G>A
  hgvsp: ENSP00000343691.3:p.Arg158Gln
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.752G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.413G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*100G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2450G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19765
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24432
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg172Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-1857473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857473
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857473
    reference: chr 11
allele count: 1
allele frequency: 1.521884702014975e-5
allele num: 65708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*102G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.517G>A
  hgvsp: ENSP00000371394.3:p.Gly173Ser
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*139G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*139G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.512G>A
  hgvsp: ENSP00000371406.3:p.Gly172Ser
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1438G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.754G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.475G>A
  hgvsp: ENSP00000343691.3:p.Gly159Ser
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2452G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.215G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.415G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.936G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly173Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS

http://identifiers.org/exac.variant/11-1857475-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857475
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857475
    reference: chr 11
allele count: 2
allele frequency: 3.044974269967419e-5
allele num: 65682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.217C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.756C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2454C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*141C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1440C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.477C>A
  hgvsp: ENST00000341958.3:c.477C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.519C>A
  hgvsp: ENST00000381968.3:c.519C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*141C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.417C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*104C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.514C>A
  hgvsp: ENST00000381978.3:c.514C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.938C>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7604
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly173Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

11-1857477-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857477
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857477
    reference: chr 11
allele count: 9
allele frequency: 1.376020548573525e-4
allele num: 65406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.940C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2456C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.516C>T
  hgvsp: ENSP00000371406.3:p.Thr173Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*106C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.758C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*143C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.479C>T
  hgvsp: ENSP00000343691.3:p.Thr160Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.521C>T
  hgvsp: ENSP00000371394.3:p.Thr174Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.419C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*143C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.219C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1442C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7935
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18751
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr174Met
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

11-1857478-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857478
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857478
    reference: chr 11
allele count: 110
allele frequency: 1.677442966939124e-3
allele num: 65576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1443G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.522G>A
  hgvsp: ENST00000381968.3:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.941G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*144G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.480G>A
  hgvsp: ENST00000341958.3:c.480G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.759G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.220G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*107G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.517G>A
  hgvsp: ENST00000381978.3:c.517G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*144G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.420G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2457G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23919
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18863
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 1.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
hgvs: p.Thr174Thr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-1857478-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857478
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857478
    reference: chr 11
allele count: 2
allele frequency: 3.04989630352568e-5
allele num: 65576
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1443G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*107G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.941G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.480G>T
  hgvsp: ENST00000341958.3:c.480G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*144G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.420G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.517G>T
  hgvsp: ENST00000381978.3:c.517G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.522G>T
  hgvsp: ENST00000381968.3:c.522G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.220G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2457G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.759G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*144G>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18863
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23919
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr174Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

11-1857480-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857480
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857480
    reference: chr 11
allele count: 4
allele frequency: 6.067224851352991e-5
allele num: 65928
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*146T>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.524T>G
  hgvsp: ENSP00000371394.3:p.Leu175Arg
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.519T>G
  hgvsp: ENSP00000371406.3:p.Leu174Arg
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.422T>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2459T>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.482T>G
  hgvsp: ENSP00000343691.3:p.Leu161Arg
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*109T>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.943T>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*146T>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.761T>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1445T>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.222T>G
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23919
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu175Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/11-1857484-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857484
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857484
    reference: chr 11
allele count: 2
allele frequency: 3.060537430372773e-5
allele num: 65348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*150C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.486C>A
  hgvsp: ENSP00000343691.3:p.Cys162Ter
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.226C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*113C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.947C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.426C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.523C>A
  hgvsp: ENSP00000371406.3:p.Cys175Ter
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.528C>A
  hgvsp: ENSP00000371394.3:p.Cys176Ter
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2463C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*150C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1449C>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.765C>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys176Ter
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

11-1857487-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857487
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857487
    reference: chr 11
allele count: 1
allele frequency: 1.552312946289972e-5
allele num: 64420
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.429C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.950C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1452C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*116C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.531C>G
  hgvsp: ENST00000381968.3:c.531C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.489C>G
  hgvsp: ENST00000341958.3:c.489C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.526C>G
  hgvsp: ENST00000381978.3:c.526C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2466C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.229C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.768C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*153C>G
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*153C>G
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro177Pro
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

11-1857487-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857487
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857487
    reference: chr 11
allele count: 6
allele frequency: 9.313877677739832e-5
allele num: 64420
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.531C>T
  hgvsp: ENST00000381968.3:c.531C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*116C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.526C>T
  hgvsp: ENST00000381978.3:c.526C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*153C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.489C>T
  hgvsp: ENST00000341958.3:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*153C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.229C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.768C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.950C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1452C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.429C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2466C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9186
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23686
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro177Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-1857488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857488
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857488
    reference: chr 11
allele count: 4
allele frequency: 6.191950464396285e-5
allele num: 64600
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.532G>A
  hgvsp: ENSP00000371394.3:p.Val178Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.527G>A
  hgvsp: ENSP00000371406.3:p.Val177Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.230G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2467G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*154G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.430G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*117G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.769G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.951G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.490G>A
  hgvsp: ENSP00000343691.3:p.Val164Met
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*154G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1453G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9156
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17151
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val178Met
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP

11-1857496-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857496
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857496
    reference: chr 11
allele count: 4
allele frequency: 6.421164157061675e-5
allele num: 62294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*162C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2475C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.777C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1461C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.535C>T
  hgvsp: ENST00000381978.3:c.535C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.438C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.959C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*125C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*162C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.540C>T
  hgvsp: ENST00000381968.3:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.238C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.498C>T
  hgvsp: ENST00000341958.3:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10764
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp180Asp
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

11-1857497-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857497
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857497
    reference: chr 11
allele count: 27
allele frequency: 4.371620090022991e-4
allele num: 61762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.239G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.499G>A
  hgvsp: ENSP00000343691.3:p.Glu167Lys
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*126G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.536G>A
  hgvsp: ENSP00000371406.3:p.Glu180Lys
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*163G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1462G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.960G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.541G>A
  hgvsp: ENSP00000371394.3:p.Glu181Lys
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2476G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.778G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.439G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*163G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4890
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24082
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13742
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11203
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu181Lys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

11-1857500-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857500
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857500
    reference: chr 11
allele count: 1
allele frequency: 1.634788294915808e-5
allele num: 61170
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.544A>T
  hgvsp: ENSP00000371394.3:p.Thr182Ser
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.539A>T
  hgvsp: ENSP00000371406.3:p.Thr181Ser
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*129A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2479A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.963A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.502A>T
  hgvsp: ENSP00000343691.3:p.Thr168Ser
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.442A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.781A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.242A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*166A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*166A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1465A>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11744
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr182Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

11-1857510-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857510
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857510
    reference: chr 11
allele count: 1
allele frequency: 1.751436177665686e-5
allele num: 57096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.252T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.554T>C
  hgvsp: ENSP00000371394.3:p.Phe185Ser
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.452T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*139T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*176T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.549T>C
  hgvsp: ENSP00000371406.3:p.Phe184Ser
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2489T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.512T>C
  hgvsp: ENSP00000343691.3:p.Phe171Ser
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*176T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.791T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1475T>C
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.973T>C
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6726
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe185Ser
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

11-1857513-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857513
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857513
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 56744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.455A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.794A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*142A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.557A>T
  hgvsp: ENSP00000371394.3:p.His186Leu
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*179A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1478A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2492A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.255A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.515A>T
  hgvsp: ENSP00000343691.3:p.His172Leu
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.552A>T
  hgvsp: ENSP00000371406.3:p.His185Leu
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*179A>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.976A>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6913
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24446
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His186Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-1857514-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857514
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857514
    reference: chr 11
allele count: 561
allele frequency: 9.961998792484996e-3
allele num: 56314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.256C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.553C>T
  hgvsp: ENST00000381978.3:c.553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*143C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.456C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.516C>T
  hgvsp: ENST00000341958.3:c.516C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*180C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2493C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1479C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.558C>T
  hgvsp: ENST00000381968.3:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.795C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*180C>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.977C>T
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 1.75e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 15232
  bin: 1.25e1
  variant carriers: 213
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 2.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 7021
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24362
  bin: 7.5e0
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 2.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: c.558C>T
num of homozygotes: 6
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

11-1857515-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857515
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857515
    reference: chr 11
allele count: 171
allele frequency: 3.087645805496371e-3
allele num: 55382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.516+1G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.978G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*143+1G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.553+1G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.558+1G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.256+1G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*180+1G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2494G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.796G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.457G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1480G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000414626
  ensembl transcript: ENST00000436964
  gene symbol: SYT8
  hgvsc: ENST00000436964.2:c.*181G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24398
  bin: 7.5e0
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 1.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 15661
  bin: 1.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6964
  bin: 2.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: c.558+1G>A
num of homozygotes: 1
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

11-1857532-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857532
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857532
    reference: chr 11
allele count: 3
allele frequency: 6.762544520084757e-5
allele num: 44362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.813G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.553+18G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.516+18G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.474G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2511G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*143+18G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.558+18G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1497G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.995G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*180+18G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.256+18G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23675
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16350
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

11-1857535-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857535
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857535
    reference: chr 11
allele count: 1
allele frequency: 2.436884686616629e-5
allele num: 41036
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2514T>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.516+21T>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.558+21T>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.816T>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*143+21T>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1500T>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.477T>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.553+21T>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.256+21T>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*180+21T>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.998T>A
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP

11-1857537-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857537
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857537
    reference: chr 11
allele count: 2
allele frequency: 4.878048780487805e-5
allele num: 41000
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.558+23G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*180+23G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.1000G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.553+23G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1502G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2516G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.479G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.818G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.256+23G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.516+23G>T
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*143+23G>T
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15342
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27716
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

11-1857538-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1857538
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1857538
    reference: chr 11
allele count: 1
allele frequency: 2.434748733930658e-5
allele num: 41072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371406
  ensembl transcript: ENST00000381978
  gene symbol: SYT8
  hgvsc: ENST00000381978.3:c.553+24G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000371394
  ensembl transcript: ENST00000381968
  gene symbol: SYT8
  hgvsc: ENST00000381968.3:c.558+24G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000490707
  gene symbol: SYT8
  hgvsc: ENST00000490707.1:n.2517G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479276
  gene symbol: SYT8
  hgvsc: ENST00000479276.1:n.1503G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000494431
  gene symbol: SYT8
  hgvsc: ENST00000494431.1:n.256+24G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000343691
  ensembl transcript: ENST00000341958
  gene symbol: SYT8
  hgvsc: ENST00000341958.3:c.516+24G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000405850
  ensembl transcript: ENST00000424556
  gene symbol: SYT8
  hgvsc: ENST00000424556.2:c.*143+24G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000464897
  gene symbol: SYT8
  hgvsc: ENST00000464897.1:n.819G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000483280
  gene symbol: SYT8
  hgvsc: ENST00000483280.1:n.480G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149043
  ensembl transcript: ENST00000479089
  gene symbol: SYT8
  hgvsc: ENST00000479089.1:n.1001G>A
  variant of: http://identifiers.org/hgnc/19264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149043
  ensembl protein: ENSP00000443325
  ensembl transcript: ENST00000535046
  gene symbol: SYT8
  hgvsc: ENST00000535046.1:c.*180+24G>A
  variant of: http://identifiers.org/hgnc/19264
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23903
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3146
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34941
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2746
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2934
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3381
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9024
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.25e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3916
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.57653791130186e-4
allele num: 2796
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4680
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.05e-2

QD
type: SiteQuality
SIO_000300: 1.171e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 5.99061e5

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1630
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2362
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 269
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3253
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33729
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10457
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2056
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.667033370003667e-5
allele num: 27270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3508
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.7e0

FS
type: SiteQuality
SIO_000300: 7.593e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.35e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

DP
type: SiteQuality
SIO_000300: 5.69308e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.639e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.034e0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1312
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2983
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1756
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2475
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2507
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31973
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11793
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3155
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.992972368631209e-5
allele num: 25044
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3778
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.23e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

VQSLOD
type: SiteQuality
SIO_000300: -3.943e0

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.57e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e0

QD
type: SiteQuality
SIO_000300: 1.95e0

DP
type: SiteQuality
SIO_000300: 5.41969e5

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30247
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 234
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13012
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3002
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1492
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3469
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2290
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2947
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1890
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 7.077140835102619e-4
allele num: 2826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4946
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

DP
type: SiteQuality
SIO_000300: 5.19874e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.81e-2

MQ
type: SiteQuality
SIO_000300: 5.868e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

FS
type: SiteQuality
SIO_000300: 1.768e0

VQSLOD
type: SiteQuality
SIO_000300: 7.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.739e0

QD
type: SiteQuality
SIO_000300: 9.0e0

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

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 728
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3969
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3158
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2262
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13397
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29144
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 748
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1363
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.75e1
variant carriers: 14

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2930
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4760
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 3.86215092097445e-3
allele num: 3366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22014
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 1.172e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.88e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 9.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.12518e5

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2216
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13652
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29857
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3170
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2860
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1778
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4712
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.142e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.86e-2

QD
type: SiteQuality
SIO_000300: 1.796e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.358000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

DP
type: SiteQuality
SIO_000300: 5.07497e5

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

GenotypeQuality
all individuals: 1004
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 171
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15746
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1743
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4608
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2648
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5718
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23864
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.820721769499418e-5
allele num: 17180
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3806
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.869e0

DP
type: SiteQuality
SIO_000300: 4.65132e5

VQSLOD
type: SiteQuality
SIO_000300: -3.122e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.758e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.24e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.637e0

QD
type: SiteQuality
SIO_000300: 1.928e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.43e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.88e-1

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1831
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2513
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 15853
bin: 7.5e0
variant carriers: 14

GenotypeQuality
all individuals: 5349
bin: 1.75e1
variant carriers: 17

GenotypeQuality
all individuals: 162
bin: 4.75e1
variant carriers: 13

GenotypeQuality
all individuals: 23794
bin: 2.25e1
variant carriers: 24

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 21

GenotypeQuality
all individuals: 99
bin: 7.75e1
variant carriers: 19

GenotypeQuality
all individuals: 222
bin: 6.75e1
variant carriers: 7

GenotypeQuality
all individuals: 62
bin: 8.75e1
variant carriers: 35

GenotypeQuality
all individuals: 82
bin: 7.25e1
variant carriers: 10

GenotypeQuality
all individuals: 157
bin: 4.25e1
variant carriers: 8

GenotypeQuality
all individuals: 4533
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 35

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 25

GenotypeQuality
all individuals: 74
bin: 9.25e1
variant carriers: 38

GenotypeQuality
all individuals: 1046
bin: 6.25e1
variant carriers: 14

GenotypeQuality
all individuals: 495
bin: 9.75e1
variant carriers: 355

GenotypeQuality
all individuals: 1878
bin: 3.25e1
variant carriers: 7

GenotypeQuality
all individuals: 606
bin: 3.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16664
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1906
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1754
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.690036900369004e-4
allele num: 2710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1118
num of homozygotes: 0

South Asian
type: Population
allele count: 336
allele frequency: 8.921933085501858e-2
allele num: 3766
num of homozygotes: 14

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 5.56e-1

DP
type: SiteQuality
SIO_000300: 4.6123e5

QD
type: SiteQuality
SIO_000300: 1.394e1

GenotypeDepth
all individuals: 10786
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 626
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2505
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1883
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6941
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16139
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4799
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 974
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.392227051904884e-5
allele num: 15644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1696
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.52e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

FS
type: SiteQuality
SIO_000300: 3.424e0

QD
type: SiteQuality
SIO_000300: 8.050000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.609e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.031e0

DP
type: SiteQuality
SIO_000300: 4.53834e5

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4651
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1822
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 980
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16300
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2466
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5632
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 23642
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 211
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.022974607013301e-4
allele num: 3308
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 946
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 6.417661404184315e-4
allele num: 15582
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

QD
type: SiteQuality
SIO_000300: 1.24e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 5.826e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.51e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.53273e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4619
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16388
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4457
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24859
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 142
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 934
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3258
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1574
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.55e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.37e-1

MQ
type: SiteQuality
SIO_000300: 5.811e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

FS
type: SiteQuality
SIO_000300: 6.622e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.7e-2

DP
type: SiteQuality
SIO_000300: 4.53502e5

VQSLOD
type: SiteQuality
SIO_000300: -1.435e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.62e-1

QD
type: SiteQuality
SIO_000300: 1.381e1

GenotypeDepth
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1267
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1384
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 85
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16977
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2393
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1729
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25849
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4095
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4000
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14756
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.39e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.46e0

DP
type: SiteQuality
SIO_000300: 4.48149e5

FS
type: SiteQuality
SIO_000300: 1.1486e1

VQSLOD
type: SiteQuality
SIO_000300: -1.331e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

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

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 480
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4021
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16991
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26452
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3604
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.75e1
variant carriers: 4

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 2.025931928687196e-4
allele num: 14808
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.418485237483953e-4
allele num: 1558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.095e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.47e-2

FS
type: SiteQuality
SIO_000300: 2.574e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 4.49273e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9307
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16991
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26452
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3604
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4021
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 85
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1474
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 6.868131868131869e-4
allele num: 1456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3102
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.47e-2

QD
type: SiteQuality
SIO_000300: 1.095e1

DP
type: SiteQuality
SIO_000300: 4.49273e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 2.574e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

GenotypeDepth
all individuals: 1178
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26452
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3604
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16991
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4021
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.75310642895732e-5
allele num: 14808
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.095e1

FS
type: SiteQuality
SIO_000300: 2.574e0

DP
type: SiteQuality
SIO_000300: 4.49273e5

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.47e-2

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25463
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4207
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 485
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1711
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17123
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2365
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4144
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.82407533779173e-5
allele num: 14654
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.41e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.57e0

VQSLOD
type: SiteQuality
SIO_000300: -7.685e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.016e0

MQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.074e0

DP
type: SiteQuality
SIO_000300: 4.48455e5

GenotypeDepth
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1713
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25952
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17126
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3905
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4084
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2365
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.790710308298248e-5
allele num: 14726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2656
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3044
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1548
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.29e-1

QD
type: SiteQuality
SIO_000300: 1.728e1

DP
type: SiteQuality
SIO_000300: 4.49725e5

VQSLOD
type: SiteQuality
SIO_000300: -9.655e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

FS
type: SiteQuality
SIO_000300: 3.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.35e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.29e-1

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1215
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25081
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17167
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4437
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1549
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1705
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14628
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1380
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.622516556291391e-4
allele num: 1510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3022
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.45e0

VQSLOD
type: SiteQuality
SIO_000300: -1.036e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.367e0

MQ
type: SiteQuality
SIO_000300: 5.643e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

DP
type: SiteQuality
SIO_000300: 4.48697e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.39e-2

GenotypeDepth
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1707
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4156
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 485
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1166
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17157
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3956
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2698
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 3.410175965079798e-4
allele num: 14662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2978
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.219e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.024e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.38e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

DP
type: SiteQuality
SIO_000300: 4.50499e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.457e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.54e-1

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16570
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5309
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4571
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1524
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23853
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2810
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14242
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.36e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

VQSLOD
type: SiteQuality
SIO_000300: -4.595e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.537e0

QD
type: SiteQuality
SIO_000300: 8.93e0

DP
type: SiteQuality
SIO_000300: 4.55227e5

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4991
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2336
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1942
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1552
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 24609
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4397
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 591
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16166
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 71
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 7.092198581560284e-4
allele num: 2820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2764
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14254
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.239e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.568e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.33e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-2

DP
type: SiteQuality
SIO_000300: 4.59614e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3724
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2379
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3959
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15696
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26988
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 672
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1334
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.827802813054759e-5
allele num: 14646
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.206e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.12e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.396e-1

QD
type: SiteQuality
SIO_000300: 7.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 4.68355e5

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3139
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31954
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2584
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2558
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3212
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11336
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.08071472581639e-4
allele num: 3246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16810
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1664
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.006e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

FS
type: SiteQuality
SIO_000300: 3.245e0

DP
type: SiteQuality
SIO_000300: 5.16607e5

VQSLOD
type: SiteQuality
SIO_000300: 4.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-2

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33910
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2136
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2566
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9930
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.714285714285714e-5
allele num: 17500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.322e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

DP
type: SiteQuality
SIO_000300: 5.35376e5

QD
type: SiteQuality
SIO_000300: 1.043e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeDepth
all individuals: 3
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4029
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 218
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34478
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9420
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2238
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2549
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 74
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 110
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 6
allele frequency: 1.693958215697346e-3
allele num: 3542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 2.814998311001013e-4
allele num: 17762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1794
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.43043e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.06e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 8.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

GenotypeDepth
all individuals: 9024
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1412
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2612
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35520
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2176
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 541
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7267
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 968
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.11522633744856e-4
allele num: 2430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3928
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.65e0

QD
type: SiteQuality
SIO_000300: 1.292e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 5.79356e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.67e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 324
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35520
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1522
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2176
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1008
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2286
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7267
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 9.75e1
variant carriers: 52

GenotypeQuality
all individuals: 150
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 264
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2612
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 135
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 541
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5121
bin: 6.25e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 968
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 50
allele frequency: 2.484348603796085e-3
allele num: 20126
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 8.230452674897119e-4
allele num: 2430
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 1.10803324099723e-3
allele num: 3610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3928
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.67e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.65e0

QD
type: SiteQuality
SIO_000300: 1.292e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

DP
type: SiteQuality
SIO_000300: 5.79356e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2395
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5846
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1876
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2538
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6597
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35690
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 138
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2826
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 7.780082987551867e-4
allele num: 3856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22350
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.49e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.286e1

FS
type: SiteQuality
SIO_000300: 2.675e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 6.14915e5

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2367
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35712
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1754
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2545
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5636
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7034
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 525
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 123
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1161
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 4.524886877828054e-4
allele num: 4420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2918
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.362240446693422e-5
allele num: 22924
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2396
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

FS
type: SiteQuality
SIO_000300: 4.015e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.22052e5

QD
type: SiteQuality
SIO_000300: 9.41e0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2536
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5461
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2397
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35740
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 344
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3960
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1236
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3028
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 1.763668430335097e-3
allele num: 4536
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

DP
type: SiteQuality
SIO_000300: 6.28257e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.32e-2

FS
type: SiteQuality
SIO_000300: 2.551e0

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.25e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1546
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7736
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 460
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35673
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5309
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2375
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2532
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4006
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.968253968253968e-4
allele num: 2520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3114
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.27e-2

FS
type: SiteQuality
SIO_000300: 4.684e0

DP
type: SiteQuality
SIO_000300: 6.32873e5

QD
type: SiteQuality
SIO_000300: 2.275e1

MQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: -2.317e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2536
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35368
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5063
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 153
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7987
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4066
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24502
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.587e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

QD
type: SiteQuality
SIO_000300: 1.031e1

VQSLOD
type: SiteQuality
SIO_000300: 5.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.51e-1

DP
type: SiteQuality
SIO_000300: 6.41656e5

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

GenotypeDepth
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1339
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2493
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8852
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4741
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 885
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 367
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35474
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.188683730882003e-4
allele num: 25238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4816
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.652e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.563e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.14e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.23e-1

DP
type: SiteQuality
SIO_000300: 6.52798e5

QD
type: SiteQuality
SIO_000300: 8.25e0

GenotypeDepth
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8878
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 697
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 417
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34984
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4661
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1515
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 7
allele frequency: 2.058823529411765e-3
allele num: 3400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 7.374631268436578e-4
allele num: 1356
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.420135527589545e-4
allele num: 4132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2722
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 3.530796390741468e-4
allele num: 25490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4816
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.244e1

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

FS
type: SiteQuality
SIO_000300: 5.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

DP
type: SiteQuality
SIO_000300: 6.59161e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.23e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 40
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 133
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 164
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 10005
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 384
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4396
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35049
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2396
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 130
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2820
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 7.146260123868509e-4
allele num: 4198
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.779321845469705e-4
allele num: 3598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 5.297010972379871e-4
allele num: 26430
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.215e1

FS
type: SiteQuality
SIO_000300: 5.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 6.71691e5

VQSLOD
type: SiteQuality
SIO_000300: 3.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 11949
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 167
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 181
bin: 9.75e1
variant carriers: 33

GenotypeQuality
all individuals: 712
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 324
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33573
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3763
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2265
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 422
bin: 5.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 31
allele frequency: 1.065585040560979e-3
allele num: 29092
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 4.921259842519685e-4
allele num: 4064
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3182
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1576
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.482294935006724e-4
allele num: 4462
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

FS
type: SiteQuality
SIO_000300: 5.590000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.09234e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

QD
type: SiteQuality
SIO_000300: 1.022e1

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

GenotypeDepth
all individuals: 383
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33016
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3457
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 300
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13053
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1700
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.282563025210084e-5
allele num: 30464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4624
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.813e0

DP
type: SiteQuality
SIO_000300: 7.28778e5

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 136
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1811
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3068
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2052
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 295
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 982
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15602
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31670
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 4.25e1
variant carriers: 1

Latino
type: Population
allele count: 2
allele frequency: 4.07000407000407e-4
allele num: 4914
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1852
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.721170395869191e-4
allele num: 5810
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 6.365951255001819e-4
allele num: 32988
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

FS
type: SiteQuality
SIO_000300: 1.843e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.208e1

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.1e-3

DP
type: SiteQuality
SIO_000300: 7.67546e5

GenotypeDepth
all individuals: 15812
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16252
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1752
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3018
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31227
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5860
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.981870229007633e-5
allele num: 33536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4918
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.7e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

FS
type: SiteQuality
SIO_000300: 2.767e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.706e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.55e-1

DP
type: SiteQuality
SIO_000300: 7.79117e5

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1674
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30936
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17031
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1907
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2846
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3934
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.883948756593821e-4
allele num: 5308
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5996
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34662
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1964
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-3

MQ
type: SiteQuality
SIO_000300: 5.933e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.409999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 7.89025e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1729
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2648
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1799
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18149
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29412
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2122
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5842
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.714293469409913e-5
allele num: 36842
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.2197e5

QD
type: SiteQuality
SIO_000300: 6.25e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

MQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.775e0

VQSLOD
type: SiteQuality
SIO_000300: -1.982e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

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

GenotypeDepth
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2568
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1680
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 288
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28388
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20812
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2260
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.163555836760519e-4
allele num: 6322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38636
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 8.49007e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 1.09e1

GenotypeDepth
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1644
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27965
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2632
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 237
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20788
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2306
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5648
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.177629488401653e-4
allele num: 6294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

QD
type: SiteQuality
SIO_000300: 7.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.059e-1

DP
type: SiteQuality
SIO_000300: 8.54764e5

ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-1

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19385
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2772
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27873
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 916
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1208
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4588
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.946e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.307e0

FS
type: SiteQuality
SIO_000300: 6.854e0

MQ
type: SiteQuality
SIO_000300: 5.766e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

DP
type: SiteQuality
SIO_000300: 8.49834e5

QD
type: SiteQuality
SIO_000300: 6.07e0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 472
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27691
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2843
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20067
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 243
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1686
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 2.314814814814815e-3
allele num: 432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4614
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 1.069355331500153e-3
allele num: 6546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6176
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.56854e5

QD
type: SiteQuality
SIO_000300: 9.65e0

FS
type: SiteQuality
SIO_000300: 1.275e0

VQSLOD
type: SiteQuality
SIO_000300: 8.120000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

GenotypeDepth
all individuals: 476
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20448
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 163
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1663
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1222
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27714
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2891
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 398
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.037783375314862e-5
allele num: 39700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6180
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.02571860816944e-4
allele num: 6610
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.57122905027933e-3
allele num: 5728
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.58643e5

FS
type: SiteQuality
SIO_000300: 8.266e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

QD
type: SiteQuality
SIO_000300: 1.03e1

VQSLOD
type: SiteQuality
SIO_000300: 9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

GenotypeDepth
all individuals: 1887
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3012
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27718
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1721
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19624
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.512436560976835e-5
allele num: 39802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2382
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: 8.9e-2

DP
type: SiteQuality
SIO_000300: 8.53948e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.19e-1

FS
type: SiteQuality
SIO_000300: 1.204e0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3097
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1223
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 296
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27688
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5980
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.995805871779509e-4
allele num: 6676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39838
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e-1

DP
type: SiteQuality
SIO_000300: 8.55115e5

BaseQRankSum
type: SiteQuality
SIO_000300: -9.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.714e0

QD
type: SiteQuality
SIO_000300: 5.13e0

MQRankSum
type: SiteQuality
SIO_000300: 7.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27632
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1757
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1194
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 3278
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18836
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1309
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 6
allele frequency: 1.02880658436214e-3
allele num: 5832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.548689044335967e-5
allele num: 39742
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5692
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

FS
type: SiteQuality
SIO_000300: 1.2851e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.33e-1

DP
type: SiteQuality
SIO_000300: 8.49314e5

VQSLOD
type: SiteQuality
SIO_000300: -1.179e0

QD
type: SiteQuality
SIO_000300: 9.51e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 174
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 301
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1712
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 19426
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 27628
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1283
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3293
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 318
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 255
bin: 9.75e1
variant carriers: 105

GenotypeQuality
all individuals: 988
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 570
bin: 4.75e1
variant carriers: 2

Other
type: Population
allele count: 2
allele frequency: 4.651162790697674e-3
allele num: 430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.256849831582123e-4
allele num: 39782
num of homozygotes: 0

Latino
type: Population
allele count: 11
allele frequency: 1.639833035181872e-3
allele num: 6708
num of homozygotes: 0

African
type: Population
allele count: 92
allele frequency: 1.604464597139867e-2
allele num: 5734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5868
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.79e0

QD
type: SiteQuality
SIO_000300: 1.166e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.13e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

FS
type: SiteQuality
SIO_000300: 5.21e-1

DP
type: SiteQuality
SIO_000300: 8.53803e5

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

GenotypeDepth
all individuals: 11
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3293
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 255
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 226
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19426
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27628
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1283
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.513699663164245e-5
allele num: 39782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5734
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.704158145875937e-4
allele num: 5868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

FS
type: SiteQuality
SIO_000300: 5.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.53803e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.166e1

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27990
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1279
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 229
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3355
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20108
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40032
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5878
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4674
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 6.995452955578874e-4
allele num: 5718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2452
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

DP
type: SiteQuality
SIO_000300: 8.50068e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-1

QD
type: SiteQuality
SIO_000300: 9.41e0

GenotypeDepth
all individuals: 496
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 430
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3666
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2430
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.764913519237557e-4
allele num: 5666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5690
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6692
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4668
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.513952436019911e-5
allele num: 39778
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

QD
type: SiteQuality
SIO_000300: 2.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.395e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.603e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-1

DP
type: SiteQuality
SIO_000300: 8.42555e5

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1827
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3998
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28318
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 92
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17899
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5370
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.506931886678722e-4
allele num: 6636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 1.037e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 8.29034e5

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 296
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1827
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 586
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 752
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3998
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17899
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28318
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 3.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5632
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 1.11731843575419e-3
allele num: 5370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2406
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.29034e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.037e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28560
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4034
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 9.75e1
variant carriers: 4

African
type: Population
allele count: 1
allele frequency: 1.77430801987225e-4
allele num: 5636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.604948286351652e-5
allele num: 39448
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

QD
type: SiteQuality
SIO_000300: 1.03e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.047e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.289e0

DP
type: SiteQuality
SIO_000300: 8.29909e5

GenotypeDepth
all individuals: 8
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16004
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29925
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4770
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4468
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.561524047470331e-4
allele num: 6404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.821869948375658e-5
allele num: 38354
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.63e-1

DP
type: SiteQuality
SIO_000300: 7.93389e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.01e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

QD
type: SiteQuality
SIO_000300: 9.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30172
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15041
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4973
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2136
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 531
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 178
bin: 9.75e1
variant carriers: 27

GenotypeQuality
all individuals: 83
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 5.252376700456957e-4
allele num: 38078
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.837559720690923e-4
allele num: 5442
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 6.309148264984228e-4
allele num: 6340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2356
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 4.212299915754001e-4
allele num: 4748
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.06e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.28e0

QD
type: SiteQuality
SIO_000300: 1.051e1

DP
type: SiteQuality
SIO_000300: 7.82575e5

GenotypeDepth
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3547
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14685
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1512
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30649
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5213
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.649287341705081e-5
allele num: 37746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4668
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4354
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5414
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

DP
type: SiteQuality
SIO_000300: 7.72284e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

QD
type: SiteQuality
SIO_000300: 1.025e1

GenotypeDepth
all individuals: 8
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14771
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1608
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6831
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32643
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2681
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9359
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2182
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5164
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.819124943617501e-5
allele num: 35472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5750
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.29e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

VQSLOD
type: SiteQuality
SIO_000300: -1.611e0

DP
type: SiteQuality
SIO_000300: 6.99661e5

FS
type: SiteQuality
SIO_000300: 1.2692e1

QD
type: SiteQuality
SIO_000300: 1.111e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33227
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9454
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7053
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 773
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2690
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5698
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4050
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.48e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.318e0

DP
type: SiteQuality
SIO_000300: 6.93093e5

MQ
type: SiteQuality
SIO_000300: 5.705e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.37e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.221e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

GenotypeDepth
all individuals: 10
bin: 9.75e1
variant carriers: 7

GenotypeDepth
all individuals: 7
bin: 7.25e1
variant carriers: 3

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1143
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1818
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 159
bin: 7.25e1
variant carriers: 16

GenotypeQuality
all individuals: 2663
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 99
bin: 8.25e1
variant carriers: 23

GenotypeQuality
all individuals: 622
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 206
bin: 5.75e1
variant carriers: 11

GenotypeQuality
all individuals: 132
bin: 7.75e1
variant carriers: 17

GenotypeQuality
all individuals: 33050
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 9066
bin: 6.25e1
variant carriers: 6

GenotypeQuality
all individuals: 791
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 7160
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 703
bin: 9.75e1
variant carriers: 555

GenotypeQuality
all individuals: 696
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 276
bin: 5.25e1
variant carriers: 17

GenotypeQuality
all individuals: 59
bin: 9.25e1
variant carriers: 19

GenotypeQuality
all individuals: 54
bin: 8.75e1
variant carriers: 22

GenotypeQuality
all individuals: 918
bin: 1.25e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 5
allele frequency: 2.332089552238806e-3
allele num: 2144
num of homozygotes: 0

African
type: Population
allele count: 22
allele frequency: 4.310344827586207e-3
allele num: 5104
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 1.428571428571429e-2
allele num: 350
num of homozygotes: 0

Latino
type: Population
allele count: 55
allele frequency: 9.710451977401131e-3
allele num: 5664
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.50501002004008e-4
allele num: 3992
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 372
allele frequency: 1.062492859590997e-2
allele num: 35012
num of homozygotes: 4

South Asian
type: Population
allele count: 101
allele frequency: 2.49505928853755e-2
allele num: 4048
num of homozygotes: 2

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.261e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.63e0

DP
type: SiteQuality
SIO_000300: 6.9051e5

QD
type: SiteQuality
SIO_000300: 1.333e1

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 9.75e1
variant carriers: 205

GenotypeQuality
all individuals: 239
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7637
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 210
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2760
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1260
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8291
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 79
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 769
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33457
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1032
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 5.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 5
allele frequency: 2.369668246445498e-3
allele num: 2110
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.958579881656805e-3
allele num: 338
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 1.380670611439842e-3
allele num: 5070
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3982
num of homozygotes: 0

Latino
type: Population
allele count: 11
allele frequency: 1.974865350089767e-3
allele num: 5570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 134
allele frequency: 3.894216797442604e-3
allele num: 34410
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 3.331624807790876e-3
allele num: 3902
num of homozygotes: 1

VQSLOD
type: SiteQuality
SIO_000300: 2.71e0

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

FS
type: SiteQuality
SIO_000300: 1.253e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.57e-1

DP
type: SiteQuality
SIO_000300: 6.75696e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.35e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.15e-1

QD
type: SiteQuality
SIO_000300: 1.633e1

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29197
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3048
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 13516
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2547
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3166
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.481894150417827e-4
allele num: 2872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.545596369309318e-5
allele num: 28204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1528
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.391200382592061e-4
allele num: 4182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

QD
type: SiteQuality
SIO_000300: 1.023e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.61e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.71e-1

FS
type: SiteQuality
SIO_000300: 1.104e0

DP
type: SiteQuality
SIO_000300: 5.53464e5

ClippingRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

GenotypeQuality
all individuals: 763
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3308
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26965
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3236
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 71
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2883
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15158
bin: 7.5e0
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.800258417572395e-5
allele num: 26314
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2592
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.78e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e0

VQSLOD
type: SiteQuality
SIO_000300: -3.735e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.246e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.359e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.52e0

MQRankSum
type: SiteQuality
SIO_000300: -7.93e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

DP
type: SiteQuality
SIO_000300: 5.28277e5

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2655
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15285
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2070
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3188
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 728
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2830
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2702
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.608242044861763e-4
allele num: 3834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1358
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.539360081259522e-4
allele num: 3938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26286
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2604
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.31e0

VQSLOD
type: SiteQuality
SIO_000300: -2.688e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.793e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.81e-2

DP
type: SiteQuality
SIO_000300: 5.26779e5

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15364
bin: 7.5e0
variant carriers: 0