22-26689003-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689003
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689003
    reference: chr 22
allele count: 1
allele frequency: 8.402090440101497e-6
allele num: 119018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.726G>T
  hgvsp: ENST00000529632.2:c.726G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.45G>T
  hgvsp: ENST00000402979.1:c.45G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.45G>T
  hgvsp: ENST00000403121.1:c.45G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.726G>T
  hgvsp: ENST00000343706.4:c.726G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.726G>T
  hgvsp: ENST00000404234.3:c.726G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.726G>T
  hgvsp: ENST00000248933.6:c.726G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.726G>T
  hgvsp: ENST00000360929.3:c.726G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5857
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu242Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

22-26689004-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689004
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689004
    reference: chr 22
allele count: 1
allele frequency: 8.399690891375198e-6
allele num: 119052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.727A>T
  hgvsp: ENSP00000354185.3:p.Met243Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.46A>T
  hgvsp: ENSP00000384838.1:p.Met16Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.727A>T
  hgvsp: ENSP00000437037.2:p.Met243Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.727A>T
  hgvsp: ENSP00000384772.3:p.Met243Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.46A>T
  hgvsp: ENSP00000384733.1:p.Met16Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.727A>T
  hgvsp: ENSP00000248933.6:p.Met243Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.727A>T
  hgvsp: ENSP00000342661.4:p.Met243Leu
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5872
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met243Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

22-26689007-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689007
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689007
    reference: chr 22
allele count: 1
allele frequency: 8.410004541402452e-6
allele num: 118906
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.730G>A
  hgvsp: ENSP00000248933.6:p.Asp244Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.49G>A
  hgvsp: ENSP00000384838.1:p.Asp17Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.730G>A
  hgvsp: ENSP00000384772.3:p.Asp244Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.730G>A
  hgvsp: ENSP00000342661.4:p.Asp244Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.730G>A
  hgvsp: ENSP00000354185.3:p.Asp244Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.49G>A
  hgvsp: ENSP00000384733.1:p.Asp17Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.730G>A
  hgvsp: ENSP00000437037.2:p.Asp244Asn
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49639
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asp244Asn
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/22-26689009-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689009
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689009
    reference: chr 22
allele count: 1
allele frequency: 8.411277841329655e-6
allele num: 118888
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.732C>A
  hgvsp: ENSP00000248933.6:p.Asp244Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.732C>A
  hgvsp: ENSP00000342661.4:p.Asp244Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.732C>A
  hgvsp: ENSP00000384772.3:p.Asp244Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.51C>A
  hgvsp: ENSP00000384838.1:p.Asp17Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.732C>A
  hgvsp: ENSP00000354185.3:p.Asp244Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.732C>A
  hgvsp: ENSP00000437037.2:p.Asp244Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.51C>A
  hgvsp: ENSP00000384733.1:p.Asp17Glu
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5818
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp244Glu
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum

22-26689031-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689031
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689031
    reference: chr 22
allele count: 1
allele frequency: 8.805452336086505e-6
allele num: 113566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.73G>A
  hgvsp: ENSP00000384733.1:p.Gly25Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.754G>A
  hgvsp: ENSP00000354185.3:p.Gly252Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.754G>A
  hgvsp: ENSP00000342661.4:p.Gly252Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.754G>A
  hgvsp: ENSP00000248933.6:p.Gly252Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.73G>A
  hgvsp: ENSP00000384838.1:p.Gly25Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.754G>A
  hgvsp: ENSP00000437037.2:p.Gly252Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.754G>A
  hgvsp: ENSP00000384772.3:p.Gly252Arg
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22209
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43848
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly252Arg
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

22-26689043-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689043
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689043
    reference: chr 22
allele count: 1
allele frequency: 9.544170420707032e-6
allele num: 104776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.85G>A
  hgvsp: ENSP00000384733.1:p.Glu29Lys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.766G>A
  hgvsp: ENSP00000248933.6:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.766G>A
  hgvsp: ENSP00000342661.4:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.766G>A
  hgvsp: ENSP00000437037.2:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.766G>A
  hgvsp: ENSP00000354185.3:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.766G>A
  hgvsp: ENSP00000384772.3:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.85G>A
  hgvsp: ENSP00000384838.1:p.Glu29Lys
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu256Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ

22-26689046-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689046
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689046
    reference: chr 22
allele count: 6
allele frequency: 6.056079294264893e-5
allele num: 99074
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.88G>C
  hgvsp: ENSP00000384838.1:p.Glu30Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.769G>C
  hgvsp: ENSP00000437037.2:p.Glu257Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.88G>C
  hgvsp: ENSP00000384733.1:p.Glu30Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.769G>C
  hgvsp: ENSP00000342661.4:p.Glu257Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.769G>C
  hgvsp: ENSP00000248933.6:p.Glu257Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.769G>C
  hgvsp: ENSP00000354185.3:p.Glu257Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.769G>C
  hgvsp: ENSP00000384772.3:p.Glu257Gln
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10002
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14383
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16831
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27982
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2652
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu257Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

22-26689053-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689053
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689053
    reference: chr 22
allele count: 1
allele frequency: 1.052742393936204e-5
allele num: 94990
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.95A>G
  hgvsp: ENSP00000384733.1:p.Gln32Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.776A>G
  hgvsp: ENSP00000342661.4:p.Gln259Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.776A>G
  hgvsp: ENSP00000354185.3:p.Gln259Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.776A>G
  hgvsp: ENSP00000248933.6:p.Gln259Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.95A>G
  hgvsp: ENSP00000384838.1:p.Gln32Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.776A>G
  hgvsp: ENSP00000384772.3:p.Gln259Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.776A>G
  hgvsp: ENSP00000437037.2:p.Gln259Arg
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2339
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln259Arg
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-26689060-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689060
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689060
    reference: chr 22
allele count: 1
allele frequency: 1.153801776854736e-5
allele num: 86670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.783C>T
  hgvsp: ENST00000404234.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.102C>T
  hgvsp: ENST00000403121.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.783C>T
  hgvsp: ENST00000360929.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.783C>T
  hgvsp: ENST00000343706.4:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.783C>T
  hgvsp: ENST00000248933.6:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.102C>T
  hgvsp: ENST00000402979.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.783C>T
  hgvsp: ENST00000529632.2:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18870
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr261Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

22-26689062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689062
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689062
    reference: chr 22
allele count: 1
allele frequency: 1.167351512887561e-5
allele num: 85664
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.785C>T
  hgvsp: ENSP00000248933.6:p.Thr262Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.785C>T
  hgvsp: ENSP00000342661.4:p.Thr262Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.785C>T
  hgvsp: ENSP00000384772.3:p.Thr262Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.104C>T
  hgvsp: ENSP00000384838.1:p.Thr35Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.785C>T
  hgvsp: ENSP00000354185.3:p.Thr262Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.104C>T
  hgvsp: ENSP00000384733.1:p.Thr35Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.785C>T
  hgvsp: ENSP00000437037.2:p.Thr262Ile
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16432
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30036
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr262Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

22-26689063-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689063
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689063
    reference: chr 22
allele count: 1
allele frequency: 1.169453865045024e-5
allele num: 85510
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.786T>C
  hgvsp: ENST00000360929.3:c.786T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.786T>C
  hgvsp: ENST00000529632.2:c.786T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.105T>C
  hgvsp: ENST00000403121.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.786T>C
  hgvsp: ENST00000343706.4:c.786T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.105T>C
  hgvsp: ENST00000402979.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.786T>C
  hgvsp: ENST00000404234.3:c.786T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.786T>C
  hgvsp: ENST00000248933.6:c.786T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11211
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2716
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16636
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2206
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30200
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr262Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

22-26689064-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689064
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689064
    reference: chr 22
allele count: 2
allele frequency: 2.391200382592061e-5
allele num: 83640
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.787A>G
  hgvsp: ENSP00000342661.4:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.787A>G
  hgvsp: ENSP00000384772.3:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.787A>G
  hgvsp: ENSP00000437037.2:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.106A>G
  hgvsp: ENSP00000384838.1:p.Thr36Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.787A>G
  hgvsp: ENSP00000354185.3:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.787A>G
  hgvsp: ENSP00000248933.6:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.106A>G
  hgvsp: ENSP00000384733.1:p.Thr36Ala
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2662
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2251
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr263Ala
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/22-26689065-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689065
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689065
    reference: chr 22
allele count: 1
allele frequency: 1.199385914411821e-5
allele num: 83376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.107C>A
  hgvsp: ENSP00000384733.1:p.Thr36Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.788C>A
  hgvsp: ENSP00000248933.6:p.Thr263Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.788C>A
  hgvsp: ENSP00000384772.3:p.Thr263Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.788C>A
  hgvsp: ENSP00000354185.3:p.Thr263Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.107C>A
  hgvsp: ENSP00000384838.1:p.Thr36Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.788C>A
  hgvsp: ENSP00000437037.2:p.Thr263Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.788C>A
  hgvsp: ENSP00000342661.4:p.Thr263Asn
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19850
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2512
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2291
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr263Asn
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

22-26689067-TCCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689067
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689064
    reference: chr 22
allele count: 1
allele frequency: 1.257102629858702e-5
allele num: 79548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.794_796delCCA
  hgvsp: ENSP00000437037.2:p.Thr265del
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.113_115delCCA
  hgvsp: ENSP00000384733.1:p.Thr38del
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.794_796delCCA
  hgvsp: ENSP00000342661.4:p.Thr265del
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.794_796delCCA
  hgvsp: ENSP00000384772.3:p.Thr265del
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.794_796delCCA
  hgvsp: ENSP00000354185.3:p.Thr265del
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.794_796delCCA
  hgvsp: ENSP00000248933.6:p.Thr265del
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.113_115delCCA
  hgvsp: ENSP00000384838.1:p.Thr38del
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21102
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11971
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr265del
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: TCCA
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

22-26689069-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689069
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689069
    reference: chr 22
allele count: 8
allele frequency: 1.044850194603349e-4
allele num: 76566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.792C>T
  hgvsp: ENST00000404234.3:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.111C>T
  hgvsp: ENST00000403121.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.792C>T
  hgvsp: ENST00000248933.6:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.111C>T
  hgvsp: ENST00000402979.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.792C>T
  hgvsp: ENST00000529632.2:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.792C>T
  hgvsp: ENST00000360929.3:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.792C>T
  hgvsp: ENST00000343706.4:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21709
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7297
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3907
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34261
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser264Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD

22-26689086-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689086
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689086
    reference: chr 22
allele count: 2
allele frequency: 3.449465332873405e-5
allele num: 57980
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.809C>T
  hgvsp: ENSP00000342661.4:p.Thr270Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.128C>T
  hgvsp: ENSP00000384838.1:p.Thr43Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.809C>T
  hgvsp: ENSP00000248933.6:p.Thr270Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.809C>T
  hgvsp: ENSP00000437037.2:p.Thr270Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.128C>T
  hgvsp: ENSP00000384733.1:p.Thr43Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.809C>T
  hgvsp: ENSP00000384772.3:p.Thr270Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.809C>T
  hgvsp: ENSP00000354185.3:p.Thr270Met
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20109
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8619
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4860
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2181
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 971
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr270Met
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ

22-26689087-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689087
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689087
    reference: chr 22
allele count: 4
allele frequency: 6.969369620517824e-5
allele num: 57394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.129G>A
  hgvsp: ENST00000402979.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.810G>A
  hgvsp: ENST00000248933.6:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.810G>A
  hgvsp: ENST00000404234.3:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.810G>A
  hgvsp: ENST00000529632.2:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.810G>A
  hgvsp: ENST00000343706.4:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.810G>A
  hgvsp: ENST00000360929.3:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.129G>A
  hgvsp: ENST00000403121.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20082
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2451
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2049
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9747
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr270Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

22-26689095-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689095
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689095
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 45090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.818C>T
  hgvsp: ENSP00000384772.3:p.Thr273Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.137C>T
  hgvsp: ENSP00000384838.1:p.Thr46Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.818C>T
  hgvsp: ENSP00000354185.3:p.Thr273Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.137C>T
  hgvsp: ENSP00000384733.1:p.Thr46Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.818C>T
  hgvsp: ENSP00000342661.4:p.Thr273Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.818C>T
  hgvsp: ENSP00000437037.2:p.Thr273Ile
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.818C>T
  hgvsp: ENSP00000248933.6:p.Thr273Ile
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13812
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15952
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15323
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1767
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr273Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/22-26689096-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689096
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689096
    reference: chr 22
allele count: 1
allele frequency: 2.300966405890474e-5
allele num: 43460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.819C>A
  hgvsp: ENST00000360929.3:c.819C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.819C>A
  hgvsp: ENST00000404234.3:c.819C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.138C>A
  hgvsp: ENST00000402979.1:c.138C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.819C>A
  hgvsp: ENST00000248933.6:c.819C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.138C>A
  hgvsp: ENST00000403121.1:c.138C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.819C>A
  hgvsp: ENST00000343706.4:c.819C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.819C>A
  hgvsp: ENST00000529632.2:c.819C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22377
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16047
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28141
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2032
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr273Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD

22-26689099-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689099
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689099
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 38274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.141C>T
  hgvsp: ENST00000402979.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.822C>T
  hgvsp: ENST00000343706.4:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.141C>T
  hgvsp: ENST00000403121.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.822C>T
  hgvsp: ENST00000529632.2:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.822C>T
  hgvsp: ENST00000404234.3:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.822C>T
  hgvsp: ENST00000248933.6:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.822C>T
  hgvsp: ENST00000360929.3:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22534
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25386
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17916
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2241
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1805
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3463
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr274Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ

22-26689100-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689100
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689100
    reference: chr 22
allele count: 2
allele frequency: 5.302226935312831e-5
allele num: 37720
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.823G>C
  hgvsp: ENSP00000248933.6:p.Glu275Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.142G>C
  hgvsp: ENSP00000384733.1:p.Glu48Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.823G>C
  hgvsp: ENSP00000384772.3:p.Glu275Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.823G>C
  hgvsp: ENSP00000354185.3:p.Glu275Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.823G>C
  hgvsp: ENSP00000437037.2:p.Glu275Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.823G>C
  hgvsp: ENSP00000342661.4:p.Glu275Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.142G>C
  hgvsp: ENSP00000384838.1:p.Glu48Gln
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13330
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16593
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25846
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu275Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

22-26689105-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689105
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689105
    reference: chr 22
allele count: 4441
allele frequency: 1.369242153295924e-1
allele num: 32434
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.828G>A
  hgvsp: ENST00000404234.3:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.828G>A
  hgvsp: ENST00000343706.4:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.147G>A
  hgvsp: ENST00000402979.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.828G>A
  hgvsp: ENST00000529632.2:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.828G>A
  hgvsp: ENST00000248933.6:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.147G>A
  hgvsp: ENST00000403121.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.828G>A
  hgvsp: ENST00000360929.3:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 19182
  bin: 2.5e0
  variant carriers: 280
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 2.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 11015
  bin: 1.25e1
  variant carriers: 2677
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 22220
  bin: 7.5e0
  variant carriers: 3283
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 2.25e1
  variant carriers: 179
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.75e1
  variant carriers: 794
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 2.75e1
  variant carriers: 195
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 7.25e1
  variant carriers: 97
genotype quality: GenotypeQuality
  all individuals: 1787
  bin: 1.75e1
  variant carriers: 186
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 3.25e1
  variant carriers: 130
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.25e1
  variant carriers: 233
genotype quality: GenotypeQuality
  all individuals: 19598
  bin: 7.5e0
  variant carriers: 101
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.25e1
  variant carriers: 168
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 7.75e1
  variant carriers: 133
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.75e1
  variant carriers: 198
hgvs: p.Gln276Gln
num of homozygotes: 230
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

22-26689131-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689131
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689131
    reference: chr 22
allele count: 1
allele frequency: 8.034709946970914e-5
allele num: 12446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.835+19C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.835+19C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.835+19C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.154+19C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.835+19C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.835+19C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.154+19C>T
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35342
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11449
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 34050
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7898
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 3.25e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-26689137-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689137
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689137
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 11484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.154+25C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.835+25C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.835+25C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.835+25C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.835+25C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.154+25C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.835+25C>T
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36055
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10012
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6446
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2447
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3649
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33954
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/22-26689147-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689147
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689147
    reference: chr 22
allele count: 209
allele frequency: 2.433061699650757e-2
allele num: 8590
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.835+35A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.835+35A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.154+35A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.835+35A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.154+35A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.835+35A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.835+35A>C
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8590
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 35802
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 6.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 30445
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1364
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 8.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 3.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1329
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.25e1
  variant carriers: 6
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

22-26689158-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26689158
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26689158
    reference: chr 22
allele count: 3
allele frequency: 3.095336359884441e-4
allele num: 9692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.835+46G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.154+46G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.154+46G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.835+46G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.835+46G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.835+46G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.835+46G>T
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8280
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8896
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1483
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS

22-26690214-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690214
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690214
    reference: chr 22
allele count: 4
allele frequency: 3.330169672144796e-5
allele num: 120114
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.836-44A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.836-44A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.155-44A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.836-44A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.155-44A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.836-44A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.836-44A>G
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3729
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
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: A
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

22-26690241-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690241
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690241
    reference: chr 22
allele count: 1
allele frequency: 8.285690612312537e-6
allele num: 120690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.836-17A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.836-17A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.836-17A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.155-17A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.155-17A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.836-17A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.836-17A>G
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1884
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-26690247-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690247
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690247
    reference: chr 22
allele count: 1
allele frequency: 8.271298593879239e-6
allele num: 120900
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.836-11C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.155-11C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.836-11C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.836-11C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.836-11C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.836-11C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.155-11C>G
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

22-26690275-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690275
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690275
    reference: chr 22
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.853T>C
  hgvsp: ENSP00000354185.3:p.Phe285Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.853T>C
  hgvsp: ENSP00000437037.2:p.Phe285Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.853T>C
  hgvsp: ENSP00000384772.3:p.Phe285Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.172T>C
  hgvsp: ENSP00000384838.1:p.Phe58Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.172T>C
  hgvsp: ENSP00000384733.1:p.Phe58Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.853T>C
  hgvsp: ENSP00000342661.4:p.Phe285Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.853T>C
  hgvsp: ENSP00000248933.6:p.Phe285Leu
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43411
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1897
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe285Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum

22-26690299-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690299
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690299
    reference: chr 22
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.877G>T
  hgvsp: ENSP00000437037.2:p.Asp293Tyr
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.877G>T
  hgvsp: ENSP00000342661.4:p.Asp293Tyr
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.196G>T
  hgvsp: ENSP00000384733.1:p.Asp66Tyr
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.877G>T
  hgvsp: ENSP00000248933.6:p.Asp293Tyr
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.877G>T
  hgvsp: ENSP00000384772.3:p.Asp293Tyr
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.877G>T
  hgvsp: ENSP00000354185.3:p.Asp293Tyr
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.196G>T
  hgvsp: ENSP00000384838.1:p.Asp66Tyr
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6844
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp293Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

22-26690308-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690308
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690308
    reference: chr 22
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.886G>A
  hgvsp: ENSP00000248933.6:p.Asp296Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.886G>A
  hgvsp: ENSP00000354185.3:p.Asp296Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.886G>A
  hgvsp: ENSP00000342661.4:p.Asp296Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.886G>A
  hgvsp: ENSP00000384772.3:p.Asp296Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.205G>A
  hgvsp: ENSP00000384733.1:p.Asp69Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.205G>A
  hgvsp: ENSP00000384838.1:p.Asp69Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.886G>A
  hgvsp: ENSP00000437037.2:p.Asp296Asn
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6851
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43412
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asp296Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS

22-26690309-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690309
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690309
    reference: chr 22
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.887A>T
  hgvsp: ENSP00000437037.2:p.Asp296Val
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.887A>T
  hgvsp: ENSP00000248933.6:p.Asp296Val
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.887A>T
  hgvsp: ENSP00000354185.3:p.Asp296Val
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.206A>T
  hgvsp: ENSP00000384733.1:p.Asp69Val
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.206A>T
  hgvsp: ENSP00000384838.1:p.Asp69Val
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.887A>T
  hgvsp: ENSP00000384772.3:p.Asp296Val
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.887A>T
  hgvsp: ENSP00000342661.4:p.Asp296Val
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43411
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp296Val
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

22-26690318-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690318
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690318
    reference: chr 22
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.896T>A
  hgvsp: ENSP00000342661.4:p.Leu299Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.896T>A
  hgvsp: ENSP00000437037.2:p.Leu299Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.215T>A
  hgvsp: ENSP00000384733.1:p.Leu72Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.896T>A
  hgvsp: ENSP00000354185.3:p.Leu299Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.896T>A
  hgvsp: ENSP00000384772.3:p.Leu299Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.896T>A
  hgvsp: ENSP00000248933.6:p.Leu299Gln
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.215T>A
  hgvsp: ENSP00000384838.1:p.Leu72Gln
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu299Gln
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

22-26690322-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690322
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690322
    reference: chr 22
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.900G>C
  hgvsp: ENST00000360929.3:c.900G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.900G>C
  hgvsp: ENST00000404234.3:c.900G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.219G>C
  hgvsp: ENST00000402979.1:c.219G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.900G>C
  hgvsp: ENST00000248933.6:c.900G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.900G>C
  hgvsp: ENST00000529632.2:c.900G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.900G>C
  hgvsp: ENST00000343706.4:c.900G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.219G>C
  hgvsp: ENST00000403121.1:c.219G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1897
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu300Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

22-26690330-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690330
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690330
    reference: chr 22
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.227A>G
  hgvsp: ENSP00000384733.1:p.Asn76Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.908A>G
  hgvsp: ENSP00000384772.3:p.Asn303Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.908A>G
  hgvsp: ENSP00000342661.4:p.Asn303Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.908A>G
  hgvsp: ENSP00000437037.2:p.Asn303Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.908A>G
  hgvsp: ENSP00000354185.3:p.Asn303Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.908A>G
  hgvsp: ENSP00000248933.6:p.Asn303Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.227A>G
  hgvsp: ENSP00000384838.1:p.Asn76Ser
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn303Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

22-26690333-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690333
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690333
    reference: chr 22
allele count: 5
allele frequency: 4.11834475487612e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.911A>G
  hgvsp: ENSP00000354185.3:p.Asn304Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.911A>G
  hgvsp: ENSP00000437037.2:p.Asn304Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.230A>G
  hgvsp: ENSP00000384838.1:p.Asn77Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.911A>G
  hgvsp: ENSP00000248933.6:p.Asn304Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.230A>G
  hgvsp: ENSP00000384733.1:p.Asn77Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.911A>G
  hgvsp: ENSP00000342661.4:p.Asn304Ser
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.911A>G
  hgvsp: ENSP00000384772.3:p.Asn304Ser
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6844
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43410
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn304Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

22-26690355-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690355
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690355
    reference: chr 22
allele count: 11
allele frequency: 9.061254077564335e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.252C>T
  hgvsp: ENST00000403121.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.933C>T
  hgvsp: ENST00000343706.4:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.933C>T
  hgvsp: ENST00000360929.3:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.933C>T
  hgvsp: ENST00000248933.6:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.252C>T
  hgvsp: ENST00000402979.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.933C>T
  hgvsp: ENST00000404234.3:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.933C>T
  hgvsp: ENST00000529632.2:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1892
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn311Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

22-26690356-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690356
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690356
    reference: chr 22
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.934G>A
  hgvsp: ENSP00000384772.3:p.Val312Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.934G>A
  hgvsp: ENSP00000354185.3:p.Val312Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.253G>A
  hgvsp: ENSP00000384838.1:p.Val85Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.934G>A
  hgvsp: ENSP00000342661.4:p.Val312Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.934G>A
  hgvsp: ENSP00000248933.6:p.Val312Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.253G>A
  hgvsp: ENSP00000384733.1:p.Val85Met
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.934G>A
  hgvsp: ENSP00000437037.2:p.Val312Met
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4057
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1892
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43406
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val312Met
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

22-26690368-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690368
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690368
    reference: chr 22
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.946A>G
  hgvsp: ENSP00000384772.3:p.Thr316Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.946A>G
  hgvsp: ENSP00000354185.3:p.Thr316Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.265A>G
  hgvsp: ENSP00000384733.1:p.Thr89Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.946A>G
  hgvsp: ENSP00000342661.4:p.Thr316Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.946A>G
  hgvsp: ENSP00000248933.6:p.Thr316Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.946A>G
  hgvsp: ENSP00000437037.2:p.Thr316Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.265A>G
  hgvsp: ENSP00000384838.1:p.Thr89Ala
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5464
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1892
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr316Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

22-26690388-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690388
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690388
    reference: chr 22
allele count: 3
allele frequency: 2.476023835856127e-5
allele num: 121162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.966C>T
  hgvsp: ENST00000360929.3:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.966C>T
  hgvsp: ENST00000404234.3:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.966C>T
  hgvsp: ENST00000248933.6:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.966C>T
  hgvsp: ENST00000343706.4:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.966C>T
  hgvsp: ENST00000529632.2:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.285C>T
  hgvsp: ENST00000402979.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.285C>T
  hgvsp: ENST00000403121.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu322Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

22-26690388-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690388
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690388
    reference: chr 22
allele count: 2
allele frequency: 1.650682557237418e-5
allele num: 121162
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.966C>G
  hgvsp: ENST00000248933.6:c.966C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.285C>G
  hgvsp: ENST00000403121.1:c.285C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.285C>G
  hgvsp: ENST00000402979.1:c.285C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.966C>G
  hgvsp: ENST00000529632.2:c.966C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.966C>G
  hgvsp: ENST00000343706.4:c.966C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.966C>G
  hgvsp: ENST00000360929.3:c.966C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.966C>G
  hgvsp: ENST00000404234.3:c.966C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5800
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu322Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD

22-26690398-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690398
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690398
    reference: chr 22
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.288+7C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.969+7C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.969+7C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.969+7C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.288+7C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.969+7C>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.969+7C>G
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5672
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2064
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.75e1
  variant carriers: 0
hgvs: c.969+7C>G
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

22-26690403-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690403
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690403
    reference: chr 22
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.288+12A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.969+12A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.969+12A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.969+12A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.969+12A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.288+12A>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.969+12A>G
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1852
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

22-26690407-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690407
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690407
    reference: chr 22
allele count: 37179
allele frequency: 3.074423220044654e-1
allele num: 120930
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.969+16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.288+16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.969+16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.969+16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.969+16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.288+16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.969+16T>C
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 5.25e1
  variant carriers: 1918
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 2.75e1
  variant carriers: 873
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 6.75e1
  variant carriers: 2574
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 4.25e1
  variant carriers: 1230
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 3.25e1
  variant carriers: 963
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 1.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 5543
  bin: 9.75e1
  variant carriers: 4748
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 7.75e1
  variant carriers: 2330
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 4.75e1
  variant carriers: 1569
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 1.75e1
  variant carriers: 311
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 4528
  bin: 3.75e1
  variant carriers: 1091
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 2.25e1
  variant carriers: 621
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 6.25e1
  variant carriers: 2430
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 8.25e1
  variant carriers: 1986
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 9.25e1
  variant carriers: 1309
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 7.25e1
  variant carriers: 2507
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 8.75e1
  variant carriers: 1733
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 5.75e1
  variant carriers: 2274
genotype quality: GenotypeQuality
  all individuals: 3765
  bin: 6.25e1
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 7.75e1
  variant carriers: 80
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 8.75e1
  variant carriers: 66
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1598
  bin: 8.25e1
  variant carriers: 85
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 3
num of homozygotes: 6629
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-26690426-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690426
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690426
    reference: chr 22
allele count: 1
allele frequency: 8.3099270388406e-6
allele num: 120338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.969+35C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.969+35C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.969+35C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.969+35C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.969+35C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.288+35C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.288+35C>A
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32394
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3345
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5448
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3746
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

22-26690426-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690426
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690426
    reference: chr 22
allele count: 2
allele frequency: 1.66198540776812e-5
allele num: 120338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.969+35C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.969+35C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.288+35C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.288+35C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.969+35C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.969+35C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.969+35C>T
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7326
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3345
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3746
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff

22-26690427-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690427
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690427
    reference: chr 22
allele count: 1
allele frequency: 8.309512730173502e-6
allele num: 120344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.969+36G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.288+36G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.969+36G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.288+36G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.969+36G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.969+36G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.969+36G>A
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3471
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

22-26690427-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690427
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690427
    reference: chr 22
allele count: 1
allele frequency: 8.309512730173502e-6
allele num: 120344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.969+36G>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.969+36G>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.288+36G>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.969+36G>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.969+36G>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.288+36G>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.969+36G>C
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3748
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-26690434-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690434
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690434
    reference: chr 22
allele count: 1
allele frequency: 8.336668000533546e-6
allele num: 119952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.969+43A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.969+43A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.969+43A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.288+43A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.288+43A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.969+43A>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.969+43A>C
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5977
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1598
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1295
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1200
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

22-26690435-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690435
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690435
    reference: chr 22
allele count: 53
allele frequency: 4.418728740078704e-4
allele num: 119944
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.969+44G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.969+44G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.969+44G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.288+44G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.969+44G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.288+44G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.969+44G>T
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7931
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6143
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32396
  bin: 9.75e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3442
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

22-26690436-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26690436
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26690436
    reference: chr 22
allele count: 2
allele frequency: 1.667389201987528e-5
allele num: 119948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.969+45G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.288+45G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.969+45G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.969+45G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.969+45G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.969+45G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.288+45G>A
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5976
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1304
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3445
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2763
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/22-26692807-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692807
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692807
    reference: chr 22
allele count: 4
allele frequency: 3.964792641344857e-5
allele num: 100888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.289-47C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.970-47C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.289-47C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.970-47C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.970-47C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.970-47C>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.970-47C>A
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14134
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15511
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12888
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3477
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3515
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6989
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6383
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

22-26692820-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692820
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692820
    reference: chr 22
allele count: 2
allele frequency: 1.956793988728867e-5
allele num: 102208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.970-34G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.289-34G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.970-34G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.289-34G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.970-34G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.970-34G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.970-34G>A
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26198
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5616
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4963
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8230
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3256
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

22-26692822-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692822
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692822
    reference: chr 22
allele count: 1
allele frequency: 9.752482006670697e-6
allele num: 102538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.970-32G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.289-32G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.970-32G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.289-32G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.970-32G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.970-32G>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.970-32G>T
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8087
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5300
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27489
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8176
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3151
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4414
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

22-26692823-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692823
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692823
    reference: chr 22
allele count: 1
allele frequency: 9.732549538677152e-6
allele num: 102748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.289-31T>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.970-31T>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.289-31T>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.970-31T>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.970-31T>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.970-31T>G
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.970-31T>G
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8035
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28676
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4157
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1511
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

22-26692826-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692826
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692826
    reference: chr 22
allele count: 2
allele frequency: 1.935059406323774e-5
allele num: 103356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.970-28C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.970-28C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.970-28C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.289-28C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.970-28C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.970-28C>T
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.289-28C>T
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7210
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4566
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

22-26692838-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692838
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692838
    reference: chr 22
allele count: 1
allele frequency: 9.369085764611089e-6
allele num: 106734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.970-16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.970-16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.970-16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.289-16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.970-16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.289-16T>C
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.970-16T>C
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33933
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38700
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7307
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1910
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

22-26692846-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692846
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692846
    reference: chr 22
allele count: 3
allele frequency: 2.749670039595249e-5
allele num: 109104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.970-8G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.289-8G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.970-8G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.970-8G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.970-8G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.970-8G>A
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.289-8G>A
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41851
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6292
  bin: 2.25e1
  variant carriers: 0
hgvs: c.970-8G>A
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

22-26692862-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692862
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692862
    reference: chr 22
allele count: 2
allele frequency: 1.768534238822864e-5
allele num: 113088
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.978T>C
  hgvsp: ENST00000360929.3:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.978T>C
  hgvsp: ENST00000404234.3:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.978T>C
  hgvsp: ENST00000248933.6:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.297T>C
  hgvsp: ENST00000402979.1:c.297T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.978T>C
  hgvsp: ENST00000343706.4:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.297T>C
  hgvsp: ENST00000403121.1:c.297T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.978T>C
  hgvsp: ENST00000529632.2:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3846
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4467
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser326Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

22-26692864-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692864
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692864
    reference: chr 22
allele count: 1
allele frequency: 8.807623879229862e-6
allele num: 113538
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.980T>C
  hgvsp: ENSP00000354185.3:p.Val327Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.299T>C
  hgvsp: ENSP00000384733.1:p.Val100Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.980T>C
  hgvsp: ENSP00000437037.2:p.Val327Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.980T>C
  hgvsp: ENSP00000342661.4:p.Val327Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.980T>C
  hgvsp: ENSP00000384772.3:p.Val327Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.980T>C
  hgvsp: ENSP00000248933.6:p.Val327Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.299T>C
  hgvsp: ENSP00000384838.1:p.Val100Ala
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4314
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val327Ala
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

22-26692869-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692869
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692869
    reference: chr 22
allele count: 7
allele frequency: 6.120700208103807e-5
allele num: 114366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.985C>T
  hgvsp: ENST00000404234.3:c.985C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.304C>T
  hgvsp: ENST00000402979.1:c.304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.304C>T
  hgvsp: ENST00000403121.1:c.304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.985C>T
  hgvsp: ENST00000529632.2:c.985C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.985C>T
  hgvsp: ENST00000360929.3:c.985C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.985C>T
  hgvsp: ENST00000248933.6:c.985C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.985C>T
  hgvsp: ENST00000343706.4:c.985C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38169
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4005
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu329Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

22-26692874-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692874
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692874
    reference: chr 22
allele count: 2
allele frequency: 1.735719368892438e-5
allele num: 115226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.990C>T
  hgvsp: ENST00000404234.3:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.309C>T
  hgvsp: ENST00000403121.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.990C>T
  hgvsp: ENST00000343706.4:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.309C>T
  hgvsp: ENST00000402979.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.990C>T
  hgvsp: ENST00000248933.6:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.990C>T
  hgvsp: ENST00000360929.3:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.990C>T
  hgvsp: ENST00000529632.2:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3507
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser330Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

22-26692875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692875
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692875
    reference: chr 22
allele count: 6
allele frequency: 5.186363322038586e-5
allele num: 115688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.991G>A
  hgvsp: ENSP00000354185.3:p.Asp331Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.310G>A
  hgvsp: ENSP00000384838.1:p.Asp104Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.991G>A
  hgvsp: ENSP00000342661.4:p.Asp331Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.991G>A
  hgvsp: ENSP00000248933.6:p.Asp331Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.991G>A
  hgvsp: ENSP00000437037.2:p.Asp331Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.991G>A
  hgvsp: ENSP00000384772.3:p.Asp331Asn
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.310G>A
  hgvsp: ENSP00000384733.1:p.Asp104Asn
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12537
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38544
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp331Asn
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

22-26692879-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692879
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692879
    reference: chr 22
allele count: 1
allele frequency: 8.590770076629668e-6
allele num: 116404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.314G>A
  hgvsp: ENSP00000384838.1:p.Gly105Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.314G>A
  hgvsp: ENSP00000384733.1:p.Gly105Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.995G>A
  hgvsp: ENSP00000342661.4:p.Gly332Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.995G>A
  hgvsp: ENSP00000437037.2:p.Gly332Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.995G>A
  hgvsp: ENSP00000248933.6:p.Gly332Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.995G>A
  hgvsp: ENSP00000384772.3:p.Gly332Glu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.995G>A
  hgvsp: ENSP00000354185.3:p.Gly332Glu
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12774
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47332
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly332Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

22-26692879-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692879
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692879
    reference: chr 22
allele count: 2
allele frequency: 1.718154015325934e-5
allele num: 116404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.995G>C
  hgvsp: ENSP00000342661.4:p.Gly332Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.995G>C
  hgvsp: ENSP00000248933.6:p.Gly332Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.995G>C
  hgvsp: ENSP00000384772.3:p.Gly332Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.995G>C
  hgvsp: ENSP00000354185.3:p.Gly332Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.995G>C
  hgvsp: ENSP00000437037.2:p.Gly332Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.314G>C
  hgvsp: ENSP00000384838.1:p.Gly105Ala
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.314G>C
  hgvsp: ENSP00000384733.1:p.Gly105Ala
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38880
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47332
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2976
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly332Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

22-26692883-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692883
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692883
    reference: chr 22
allele count: 1
allele frequency: 8.553441905022582e-6
allele num: 116912
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.999A>G
  hgvsp: ENST00000529632.2:c.999A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.999A>G
  hgvsp: ENST00000404234.3:c.999A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.999A>G
  hgvsp: ENST00000248933.6:c.999A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.318A>G
  hgvsp: ENST00000403121.1:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.999A>G
  hgvsp: ENST00000360929.3:c.999A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.999A>G
  hgvsp: ENST00000343706.4:c.999A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.318A>G
  hgvsp: ENST00000402979.1:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu333Glu
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

22-26692896-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692896
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692896
    reference: chr 22
allele count: 1
allele frequency: 8.464533604198409e-6
allele num: 118140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.1012C>T
  hgvsp: ENSP00000437037.2:p.Arg338Cys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.1012C>T
  hgvsp: ENSP00000248933.6:p.Arg338Cys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.1012C>T
  hgvsp: ENSP00000384772.3:p.Arg338Cys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.331C>T
  hgvsp: ENSP00000384733.1:p.Arg111Cys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.1012C>T
  hgvsp: ENSP00000342661.4:p.Arg338Cys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.331C>T
  hgvsp: ENSP00000384838.1:p.Arg111Cys
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.1012C>T
  hgvsp: ENSP00000354185.3:p.Arg338Cys
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13893
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2180
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4291
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg338Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD

22-26692897-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692897
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692897
    reference: chr 22
allele count: 1
allele frequency: 8.450370971285639e-6
allele num: 118338
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.1013G>A
  hgvsp: ENSP00000248933.6:p.Arg338His
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.1013G>A
  hgvsp: ENSP00000437037.2:p.Arg338His
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.1013G>A
  hgvsp: ENSP00000354185.3:p.Arg338His
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.1013G>A
  hgvsp: ENSP00000342661.4:p.Arg338His
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.332G>A
  hgvsp: ENSP00000384733.1:p.Arg111His
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.1013G>A
  hgvsp: ENSP00000384772.3:p.Arg338His
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.332G>A
  hgvsp: ENSP00000384838.1:p.Arg111His
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48082
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg338His
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

22-26692897-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692897
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692897
    reference: chr 22
allele count: 2
allele frequency: 1.690074194257128e-5
allele num: 118338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.332G>T
  hgvsp: ENSP00000384733.1:p.Arg111Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.1013G>T
  hgvsp: ENSP00000248933.6:p.Arg338Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.1013G>T
  hgvsp: ENSP00000437037.2:p.Arg338Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.1013G>T
  hgvsp: ENSP00000342661.4:p.Arg338Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.1013G>T
  hgvsp: ENSP00000354185.3:p.Arg338Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.1013G>T
  hgvsp: ENSP00000384772.3:p.Arg338Leu
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.332G>T
  hgvsp: ENSP00000384838.1:p.Arg111Leu
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg338Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

22-26692898-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692898
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692898
    reference: chr 22
allele count: 1
allele frequency: 8.447230153232754e-6
allele num: 118382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.1014C>T
  hgvsp: ENST00000343706.4:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.1014C>T
  hgvsp: ENST00000404234.3:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.1014C>T
  hgvsp: ENST00000360929.3:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.333C>T
  hgvsp: ENST00000402979.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.1014C>T
  hgvsp: ENST00000529632.2:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.1014C>T
  hgvsp: ENST00000248933.6:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.333C>T
  hgvsp: ENST00000403121.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4288
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg338Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

22-26692899-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26692899
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 26692899
    reference: chr 22
allele count: 4
allele frequency: 3.37427453097584e-5
allele num: 118544
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000248933
  ensembl transcript: ENST00000248933
  gene symbol: SEZ6L
  hgvsc: ENST00000248933.6:c.1015G>A
  hgvsp: ENSP00000248933.6:p.Gly339Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384772
  ensembl transcript: ENST00000404234
  gene symbol: SEZ6L
  hgvsc: ENST00000404234.3:c.1015G>A
  hgvsp: ENSP00000384772.3:p.Gly339Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000354185
  ensembl transcript: ENST00000360929
  gene symbol: SEZ6L
  hgvsc: ENST00000360929.3:c.1015G>A
  hgvsp: ENSP00000354185.3:p.Gly339Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384733
  ensembl transcript: ENST00000402979
  gene symbol: SEZ6L
  hgvsc: ENST00000402979.1:c.334G>A
  hgvsp: ENSP00000384733.1:p.Gly112Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000437037
  ensembl transcript: ENST00000529632
  gene symbol: SEZ6L
  hgvsc: ENST00000529632.2:c.1015G>A
  hgvsp: ENSP00000437037.2:p.Gly339Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000342661
  ensembl transcript: ENST00000343706
  gene symbol: SEZ6L
  hgvsc: ENST00000343706.4:c.1015G>A
  hgvsp: ENSP00000342661.4:p.Gly339Arg
  variant of: http://identifiers.org/hgnc/10763
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100095
  ensembl protein: ENSP00000384838
  ensembl transcript: ENST00000403121
  gene symbol: SEZ6L
  hgvsc: ENST00000403121.1:c.334G>A
  hgvsp: ENSP00000384838.1:p.Gly112Arg
  variant of: http://identifiers.org/hgnc/10763
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly339Arg
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 181
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49796
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 814
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65226
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.083465141744738e-5
allele num: 16438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.064e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.786e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 6.82e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.849e-1

DP
type: SiteQuality
SIO_000300: 1.510064e6

GenotypeQuality
all individuals: 1075
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49923
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 815
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65252
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.183431952662722e-4
allele num: 8450
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10044
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.338e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.291e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e0

VQSLOD
type: SiteQuality
SIO_000300: -9.416e-1

DP
type: SiteQuality
SIO_000300: 1.510277e6

GenotypeQuality
all individuals: 137
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5830
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.088650754992694e-5
allele num: 16424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10034
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65190
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.123e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.341e0

VQSLOD
type: SiteQuality
SIO_000300: -2.31e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

QD
type: SiteQuality
SIO_000300: 1.444e1

DP
type: SiteQuality
SIO_000300: 1.507392e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.46e-1

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

GenotypeQuality
all individuals: 49660
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534024667116647e-5
allele num: 65188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 3.226e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.346e1

MQ
type: SiteQuality
SIO_000300: 5.912e1

DP
type: SiteQuality
SIO_000300: 1.506666e6

MQRankSum
type: SiteQuality
SIO_000300: 3.89e-1

GenotypeQuality
all individuals: 689
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6468
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 687
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5044
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.040366208905535e-4
allele num: 9612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

FS
type: SiteQuality
SIO_000300: 1.0352e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.57e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.144e0

DP
type: SiteQuality
SIO_000300: 1.411638e6

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1562
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4335
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34155
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14730
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7112
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8990
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.737921445950643e-5
allele num: 57540
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

QD
type: SiteQuality
SIO_000300: 1.439e1

DP
type: SiteQuality
SIO_000300: 1.249194e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.804e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19787
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1786
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2009
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.924557351809084e-4
allele num: 5196
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 9.160864785635764e-5
allele num: 54580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.142681e6

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

FS
type: SiteQuality
SIO_000300: 1.762e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.77e-1

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 451
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1911
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23313
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2229
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25268
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4952
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.200192030724916e-4
allele num: 8332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13600
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.29e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

FS
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

DP
type: SiteQuality
SIO_000300: 1.070687e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.722e0

MQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.435e0

GenotypeQuality
all individuals: 458
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29343
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2354
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16942
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7780
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.090912892568895e-5
allele num: 47826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7850
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.043e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

FS
type: SiteQuality
SIO_000300: 3.424e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.9e-3

DP
type: SiteQuality
SIO_000300: 9.39094e5

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 9.960000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

MQ
type: SiteQuality
SIO_000300: 5.811e1

GenotypeQuality
all individuals: 1597
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2747
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.116222965251619e-5
allele num: 47254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7736
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.7896e1

MQ
type: SiteQuality
SIO_000300: 5.923e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 1.175e1

DP
type: SiteQuality
SIO_000300: 9.24746e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.81e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.643e0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2316
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 311
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47154
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7708
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.054123711340206e-5
allele num: 12416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7708
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 9.23034e5

QD
type: SiteQuality
SIO_000300: 1.165e1

VQSLOD
type: SiteQuality
SIO_000300: 4.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.8e-3

GenotypeQuality
all individuals: 316
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1429
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30546
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 497
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15219
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.329379167027448e-5
allele num: 46196
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5250
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.09132e5

MQRankSum
type: SiteQuality
SIO_000300: -8.33e-1

FS
type: SiteQuality
SIO_000300: 4.323e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 8.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e-1

GenotypeQuality
all individuals: 31649
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2733
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15453
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.91131498470948e-4
allele num: 5232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46012
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
SIO_000300: 1.541e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.533e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.96136e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3224
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33147
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2860
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.278008109708871e-5
allele num: 43898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4942
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4114
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.82e0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

MQ
type: SiteQuality
SIO_000300: 5.385e1

MQRankSum
type: SiteQuality
SIO_000300: -2.392e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.312e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

DP
type: SiteQuality
SIO_000300: 8.48038e5

GenotypeQuality
all individuals: 943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 335
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2561
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4662
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 7.103534008169064e-4
allele num: 11262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.692e0

FS
type: SiteQuality
SIO_000300: 4.791e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.820000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.1019e5

MQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

QD
type: SiteQuality
SIO_000300: 9.84e0

GenotypeQuality
all individuals: 1626
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9665
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34563
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2514
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 257
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.05698214722426e-5
allele num: 32712
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.041e1

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.15e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

DP
type: SiteQuality
SIO_000300: 6.5167e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 34945
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4941
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 96
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.182592242194891e-4
allele num: 8456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 9.263833992094861e-5
allele num: 32384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2850
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.88e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

QD
type: SiteQuality
SIO_000300: 1.181e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

DP
type: SiteQuality
SIO_000300: 6.48774e5

GenotypeQuality
all individuals: 29066
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2084
num of homozygotes: 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: 324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25930
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3250
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.215e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 5.68249e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-2

QD
type: SiteQuality
SIO_000300: 1.009e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 530
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3448
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 96
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.98215992354253e-5
allele num: 25112
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1926
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3040
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.23e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-1

DP
type: SiteQuality
SIO_000300: 5.59497e5

VQSLOD
type: SiteQuality
SIO_000300: -1.764e0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

MQ
type: SiteQuality
SIO_000300: 5.863e1

FS
type: SiteQuality
SIO_000300: 3.14e0

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

GenotypeQuality
all individuals: 1191
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1593
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 190
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3227
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22226
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: 1610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2376
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-2

QD
type: SiteQuality
SIO_000300: 1.408e1

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.33773e5

VQSLOD
type: SiteQuality
SIO_000300: 5.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 649
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2195
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 518
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 155
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1716
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.738525730180807e-4
allele num: 5752
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 6.329113924050633e-4
allele num: 1580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21916
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.484e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.06e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.30809e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

VQSLOD
type: SiteQuality
SIO_000300: -6.292e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.78e-1

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.08e-1

GenotypeQuality
all individuals: 3053
bin: 2.5e0
variant carriers: 11

GenotypeQuality
all individuals: 1321
bin: 1.25e1
variant carriers: 104

GenotypeQuality
all individuals: 556
bin: 6.75e1
variant carriers: 133

GenotypeQuality
all individuals: 251
bin: 3.75e1
variant carriers: 58

GenotypeQuality
all individuals: 4857
bin: 9.75e1
variant carriers: 4690

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 88

GenotypeQuality
all individuals: 407
bin: 8.75e1
variant carriers: 372

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 60

GenotypeQuality
all individuals: 2964
bin: 6.25e1
variant carriers: 205

GenotypeQuality
all individuals: 20196
bin: 2.25e1
variant carriers: 247

GenotypeQuality
all individuals: 442
bin: 9.25e1
variant carriers: 400

European (Finnish)
type: Population
allele count: 286
allele frequency: 2.143928035982009e-1
allele num: 1334
num of homozygotes: 17

South Asian
type: Population
allele count: 792
allele frequency: 1.549902152641879e-1
allele num: 5110
num of homozygotes: 45

Other
type: Population
allele count: 44
allele frequency: 1.732283464566929e-1
allele num: 254
num of homozygotes: 3

Latino
type: Population
allele count: 145
allele frequency: 7.975797579757976e-2
allele num: 1818
num of homozygotes: 3

African
type: Population
allele count: 96
allele frequency: 2.532981530343008e-2
allele num: 3790
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 3078
allele frequency: 1.631333474666101e-1
allele num: 18868
num of homozygotes: 161

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1260
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.14499e5

QD
type: SiteQuality
SIO_000300: 1.615e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.16e-2

GenotypeQuality
all individuals: 439
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2283
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3040
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.5359477124183e-4
allele num: 1530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.190000000000001e-2

DP
type: SiteQuality
SIO_000300: 3.13815e5

QD
type: SiteQuality
SIO_000300: 1.6e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 8.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 90
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6732
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.45e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.64e-1

DP
type: SiteQuality
SIO_000300: 2.96138e5

GenotypeQuality
all individuals: 296
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3527
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 358
bin: 9.75e1
variant carriers: 119

GenotypeQuality
all individuals: 7586
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 9

GenotypeQuality
all individuals: 3067
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 122
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 120
bin: 7.75e1
variant carriers: 5

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

African
type: Population
allele count: 75
allele frequency: 3.890041493775934e-2
allele num: 1928
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 134
allele frequency: 2.656621728786677e-2
allele num: 5044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e0

DP
type: SiteQuality
SIO_000300: 2.8474e5

FS
type: SiteQuality
SIO_000300: 3.5836e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.341e0

VQSLOD
type: SiteQuality
SIO_000300: -6.884e0

QD
type: SiteQuality
SIO_000300: 1.76e0

MQ
type: SiteQuality
SIO_000300: 5.766e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.06e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.171e0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3708
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2342
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2114
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27051
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.129958960328317e-4
allele num: 5848
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.056e0

DP
type: SiteQuality
SIO_000300: 2.79032e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.28e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.27e-1

QD
type: SiteQuality
SIO_000300: 1.109e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.713e0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1822
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43412
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1029
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.031363088057901e-5
allele num: 66320
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

DP
type: SiteQuality
SIO_000300: 3.565451e6

MQ
type: SiteQuality
SIO_000300: 5.984e1

MQRankSum
type: SiteQuality
SIO_000300: -7.39e-1

FS
type: SiteQuality
SIO_000300: 4.479e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.467e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.931e0

VQSLOD
type: SiteQuality
SIO_000300: 4.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.233e1

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2102
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5982
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43411
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1078
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16046
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66496
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.799e1

DP
type: SiteQuality
SIO_000300: 3.590854e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 1.172e0

VQSLOD
type: SiteQuality
SIO_000300: -7.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6247
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43411
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.595722e6

FS
type: SiteQuality
SIO_000300: 1.1354e1

VQSLOD
type: SiteQuality
SIO_000300: -1.682e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.967e0

QD
type: SiteQuality
SIO_000300: 9.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6809
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2247
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.69e-1

QD
type: SiteQuality
SIO_000300: 1.188e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 6.662e0

DP
type: SiteQuality
SIO_000300: 3.603467e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2252
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43412
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1118
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.53e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

FS
type: SiteQuality
SIO_000300: 1.108e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.432e0

DP
type: SiteQuality
SIO_000300: 3.604212e6

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

GenotypeQuality
all individuals: 1118
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1893
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 3.604131e6

MQ
type: SiteQuality
SIO_000300: 5.929e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.7e-1

QD
type: SiteQuality
SIO_000300: 1.663e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

FS
type: SiteQuality
SIO_000300: 1.3301e1

GenotypeQuality
all individuals: 6852
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2165
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1118
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495324862143371e-5
allele num: 66736
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 1.108e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.15e-1

DP
type: SiteQuality
SIO_000300: 3.604209e6

QD
type: SiteQuality
SIO_000300: 1.263e1

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

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6850
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43410
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 8.75e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.46e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

DP
type: SiteQuality
SIO_000300: 3.603948e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.598e1

GenotypeQuality
all individuals: 6845
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43410
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1116
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.603984e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 1.744e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: 7.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.404e0

QD
type: SiteQuality
SIO_000300: 1.297e1

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43410
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6847
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1893
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.387e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.390000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.603849e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.62e0

VQSLOD
type: SiteQuality
SIO_000300: -2.137e0

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 1.631e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.789e0

GenotypeQuality
all individuals: 2254
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.60391e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

FS
type: SiteQuality
SIO_000300: 1.755e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

QD
type: SiteQuality
SIO_000300: 1.457e1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-1

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43408
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 6818
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.498576352465158e-4
allele num: 66730
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

DP
type: SiteQuality
SIO_000300: 3.603646e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

FS
type: SiteQuality
SIO_000300: 1.153e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

QD
type: SiteQuality
SIO_000300: 1.252e1

GenotypeQuality
all individuals: 1894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1113
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6816
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -6.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.403e1

MQ
type: SiteQuality
SIO_000300: 5.901e1

FS
type: SiteQuality
SIO_000300: 1.404e0

DP
type: SiteQuality
SIO_000300: 3.602867e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.13e-1

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2166
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6764
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43405
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

MQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e0

VQSLOD
type: SiteQuality
SIO_000300: 1.15e-1

DP
type: SiteQuality
SIO_000300: 3.601886e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2086
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5800
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43390
bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16352
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499910001799964e-5
allele num: 66668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.594253e6

FS
type: SiteQuality
SIO_000300: 5.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.805e0

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.273e1

GenotypeQuality
all individuals: 2086
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1876
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43390
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999940001199976e-5
allele num: 66668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.273e1

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.805e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

FS
type: SiteQuality
SIO_000300: 5.89e-1

DP
type: SiteQuality
SIO_000300: 3.594253e6

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43386
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1851
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 2.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.136475208640157e-5
allele num: 16296
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.589945e6

QD
type: SiteQuality
SIO_000300: 1.231e1

FS
type: SiteQuality
SIO_000300: 6.983e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.065e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.17e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

GenotypeQuality
all individuals: 278
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5168
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43379
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1073
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1877
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 4.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.377e0

FS
type: SiteQuality
SIO_000300: 7.48e-1

QD
type: SiteQuality
SIO_000300: 1.728e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e0

DP
type: SiteQuality
SIO_000300: 3.586439e6

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.17e0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 143
bin: 3.75e1
variant carriers: 15

GenotypeQuality
all individuals: 1569
bin: 6.75e1
variant carriers: 73

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1888
bin: 9.25e1
variant carriers: 115

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 15

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 27

GenotypeQuality
all individuals: 863
bin: 7.25e1
variant carriers: 50

GenotypeQuality
all individuals: 47027
bin: 9.75e1
variant carriers: 29894

GenotypeQuality
all individuals: 254
bin: 3.25e1
variant carriers: 12

European (Non-Finnish)
type: Population
allele count: 26349
allele frequency: 3.956900435500826e-1
allele num: 66590
num of homozygotes: 5177

Latino
type: Population
allele count: 2608
allele frequency: 2.255665109842588e-1
allele num: 11562
num of homozygotes: 326

South Asian
type: Population
allele count: 2790
allele frequency: 1.719038817005545e-1
allele num: 16230
num of homozygotes: 286

African
type: Population
allele count: 2847
allele frequency: 2.740134744947064e-1
allele num: 10390
num of homozygotes: 382

European (Finnish)
type: Population
allele count: 2283
allele frequency: 3.456995760145367e-1
allele num: 6604
num of homozygotes: 407

East Asian
type: Population
allele count: 16
allele frequency: 1.850138760407031e-3
allele num: 8648
num of homozygotes: 0

Other
type: Population
allele count: 286
allele frequency: 3.15673289183223e-1
allele num: 906
num of homozygotes: 51

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

DP
type: SiteQuality
SIO_000300: 3.60165e6

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.41e0

FS
type: SiteQuality
SIO_000300: 1.452e0

QD
type: SiteQuality
SIO_000300: 1.907e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.99e-2

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.69e0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1741
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1332
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.656237929702588e-5
allele num: 10356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15898
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

DP
type: SiteQuality
SIO_000300: 2.739748e6

GenotypeQuality
all individuals: 745
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1741
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5448
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32394
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 2
allele frequency: 1.931247585940518e-4
allele num: 10356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66360
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15898
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

DP
type: SiteQuality
SIO_000300: 2.739748e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

GenotypeQuality
all individuals: 1741
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3343
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32386
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3748
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15888
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.658103148541626e-5
allele num: 10354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

FS
type: SiteQuality
SIO_000300: 8.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.861e0

QD
type: SiteQuality
SIO_000300: 1.183e1

DP
type: SiteQuality
SIO_000300: 2.737516e6

VQSLOD
type: SiteQuality
SIO_000300: 3.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 987
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3248
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1741
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32386
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3343
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15888
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.183e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 8.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 2.737516e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.861e0

GenotypeQuality
all individuals: 3677
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3219
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32377
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2772
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3739
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1958
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15626
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509160604871571e-5
allele num: 66262
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQRankSum
type: SiteQuality
SIO_000300: -1.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.663e0

QD
type: SiteQuality
SIO_000300: 1.397e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

FS
type: SiteQuality
SIO_000300: 5.462e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

DP
type: SiteQuality
SIO_000300: 2.721728e6

VQSLOD
type: SiteQuality
SIO_000300: 5.45e-1

GenotypeQuality
all individuals: 1133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1307
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3737
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2757
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3212
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1958
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1588
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15606
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.653513326410523e-4
allele num: 11556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.035185129303841e-5
allele num: 66278
num of homozygotes: 0

African
type: Population
allele count: 39
allele frequency: 3.77030162412993e-3
allele num: 10344
num of homozygotes: 1

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

DP
type: SiteQuality
SIO_000300: 2.721322e6

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

QD
type: SiteQuality
SIO_000300: 1.41e1

FS
type: SiteQuality
SIO_000300: 2.432e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.775e0

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

GenotypeQuality
all individuals: 108
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3739
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3214
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3877
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32378
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1958
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66270
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.402868485081316e-5
allele num: 15618
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.912e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.336e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: -2.785e0

DP
type: SiteQuality
SIO_000300: 2.720705e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.22e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
all individuals: 2430
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6706
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 5924
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14656
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1587
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3504
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.11474068264739e-5
allele num: 58654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9262
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.763718023823472e-5
allele num: 10242
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.34e-1

DP
type: SiteQuality
SIO_000300: 1.022709e6

FS
type: SiteQuality
SIO_000300: 7.857e0

VQSLOD
type: SiteQuality
SIO_000300: 3.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.216e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.735e0

GenotypeQuality
all individuals: 2111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2626
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.142245072836333e-4
allele num: 9336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8924
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59282
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.016e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.041e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.099178e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.088e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

QD
type: SiteQuality
SIO_000300: 2.253e1

GenotypeQuality
all individuals: 1689
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2709
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1626
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.681576646263537e-5
allele num: 59468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8996
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: -4.483e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

FS
type: SiteQuality
SIO_000300: 1.901e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.013e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

QD
type: SiteQuality
SIO_000300: 1.733e1

DP
type: SiteQuality
SIO_000300: 1.11574e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

GenotypeQuality
all individuals: 5095
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2732
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3063
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8199
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 287
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9026
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.232134056185313e-4
allele num: 8116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59572
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.377e1

DP
type: SiteQuality
SIO_000300: 1.124738e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

FS
type: SiteQuality
SIO_000300: 2.795e0

MQRankSum
type: SiteQuality
SIO_000300: 8.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.022e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

GenotypeQuality
all individuals: 31635
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2883
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8303
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9222
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.129018522461145e-4
allele num: 9394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59840
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

DP
type: SiteQuality
SIO_000300: 1.150072e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.156e0

VQSLOD
type: SiteQuality
SIO_000300: -1.517e0

FS
type: SiteQuality
SIO_000300: 1.323e0

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

QD
type: SiteQuality
SIO_000300: 2.286e1

GenotypeQuality
all individuals: 423
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1500
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2530
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10762
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.049538203190596e-4
allele num: 9528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.67e-1

FS
type: SiteQuality
SIO_000300: 2.09e0

QD
type: SiteQuality
SIO_000300: 2.48e0

MQRankSum
type: SiteQuality
SIO_000300: -2.33e-1

DP
type: SiteQuality
SIO_000300: 1.23899e6

VQSLOD
type: SiteQuality
SIO_000300: -1.907e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.643e1

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3521
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9678
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.792944785276074e-5
allele num: 62592
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.012e0

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

QD
type: SiteQuality
SIO_000300: 1.373e1

DP
type: SiteQuality
SIO_000300: 1.284836e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

FS
type: SiteQuality
SIO_000300: 3.31e0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

GenotypeQuality
all individuals: 610
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44807
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.010305112143867e-4
allele num: 9898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56137775973519e-5
allele num: 64046
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 1.425e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.143e1

DP
type: SiteQuality
SIO_000300: 1.339741e6

GenotypeQuality
all individuals: 764
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3935
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45316
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5980
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557438325442313e-5
allele num: 64208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12842
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 1.343526e6

VQSLOD
type: SiteQuality
SIO_000300: -8.87e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e-1

QD
type: SiteQuality
SIO_000300: 6.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 904
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3918
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 9.75e1
variant carriers: 7

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13276
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.1547064305685e-4
allele num: 8584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11236
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.325e0

DP
type: SiteQuality
SIO_000300: 1.35422e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.021e0

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.63e-1

QD
type: SiteQuality
SIO_000300: 1.064e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.88e-1

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

GenotypeQuality
all individuals: 553
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 957
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45935
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.869966294128082e-5
allele num: 11274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545881770962157e-5
allele num: 64688
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6034
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13764
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 4.537e0

VQSLOD
type: SiteQuality
SIO_000300: 4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.211e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.133e1

DP
type: SiteQuality
SIO_000300: 1.366953e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.54e-1

GenotypeQuality
all individuals: 251
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46722
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4131
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64826
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.137056560763641e-4
allele num: 14038
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.771793054571226e-4
allele num: 11288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6052
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.13e-1

FS
type: SiteQuality
SIO_000300: 2.088e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

DP
type: SiteQuality
SIO_000300: 1.372537e6

QD
type: SiteQuality
SIO_000300: 1.107e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4175
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2976
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 2.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14464
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.054e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

MQ
type: SiteQuality
SIO_000300: 5.904e1

VQSLOD
type: SiteQuality
SIO_000300: 4.7e-2

DP
type: SiteQuality
SIO_000300: 1.380647e6

FS
type: SiteQuality
SIO_000300: 1.685e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.42e-1

GenotypeQuality
all individuals: 4175
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.075030750307503e-5
allele num: 65040
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.7e-2

DP
type: SiteQuality
SIO_000300: 1.380647e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.42e-1

MQ
type: SiteQuality
SIO_000300: 5.904e1

FS
type: SiteQuality
SIO_000300: 1.685e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

QD
type: SiteQuality
SIO_000300: 1.054e1

GenotypeQuality
all individuals: 47291
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4221
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 354
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533836431682925e-5
allele num: 65196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.143e0

MQRankSum
type: SiteQuality
SIO_000300: 4.18e-1

QD
type: SiteQuality
SIO_000300: 1.685e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -9.515e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.377e0

DP
type: SiteQuality
SIO_000300: 1.38495e6

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

GenotypeQuality
all individuals: 525
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 772
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65556
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6140
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.466632177961717e-5
allele num: 15464
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.818e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.403462e6

VQSLOD
type: SiteQuality
SIO_000300: -1.218e-1

FS
type: SiteQuality
SIO_000300: 4.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.12e-1

QD
type: SiteQuality
SIO_000300: 8.630000000000001e0

GenotypeQuality
all individuals: 612
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 984
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 156
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4318
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523879186858066e-5
allele num: 65622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15558
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 8.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.949e1

DP
type: SiteQuality
SIO_000300: 1.405275e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.98e-1

GenotypeQuality
all individuals: 48082
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.047758373716132e-5
allele num: 65622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.949e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

FS
type: SiteQuality
SIO_000300: 7.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.98e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.8e-3

DP
type: SiteQuality
SIO_000300: 1.405275e6

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 8.23e0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2115
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47360
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523229246001523e-5
allele num: 65650
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.405947e6

MQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

FS
type: SiteQuality
SIO_000300: 1.298e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.794e-1

QD
type: SiteQuality
SIO_000300: 5.62e0