17-38068800-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38068800
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38068800
    reference: chr 17
allele count: 1
allele frequency: 8.352404657300837e-6
allele num: 119726
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.236-50A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.67-50A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.236-50A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.236-50A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.236-50A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2774-50A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.236-50A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.236-50A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.236-50A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.236-50A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.236-50A>C
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14616
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

17-38073289-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073289
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073289
    reference: chr 17
allele count: 3
allele frequency: 2.498917135907773e-5
allele num: 120052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.235+46C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2773+46C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.66+46C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.235+46C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.235+46C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.235+46C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.235+46C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.235+46C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.235+46C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.235+46C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.235+46C>T
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12967
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11082
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

17-38073290-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073290
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073290
    reference: chr 17
allele count: 1
allele frequency: 8.324453915823122e-6
allele num: 120128
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.235+45C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.235+45C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2773+45C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.235+45C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.66+45C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.235+45C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.235+45C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.235+45C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.235+45C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.235+45C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.235+45C>A
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP

17-38073295-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073295
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073295
    reference: chr 17
allele count: 5
allele frequency: 4.156483282624237e-5
allele num: 120294
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.235+40C>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2773+40C>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.235+40C>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.66+40C>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.235+40C>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.235+40C>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.235+40C>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.235+40C>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.235+40C>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.235+40C>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.235+40C>G
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16661
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11397
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

17-38073308-GCCACCTGTCAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073308
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073297
    reference: chr 17
allele count: 2
allele frequency: 1.653493832468005e-5
allele num: 120956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3194
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: GCCACCTGTCAT
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-38073319-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073319
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073319
    reference: chr 17
allele count: 6
allele frequency: 4.947229551451187e-5
allele num: 121280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.235+16A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.235+16A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.235+16A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.235+16A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.235+16A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.235+16A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.235+16A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.235+16A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2773+16A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.66+16A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.235+16A>G
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8500
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

17-38073323-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073323
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073323
    reference: chr 17
allele count: 5
allele frequency: 4.121128200056047e-5
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.235+12G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.235+12G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.235+12G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.235+12G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.235+12G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2773+12G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.235+12G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.235+12G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.66+12G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.235+12G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.235+12G>A
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2028
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

17-38073328-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073328
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073328
    reference: chr 17
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.235+7A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2773+7A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.235+7A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.235+7A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.235+7A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.66+7A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.235+7A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.235+7A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.235+7A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.235+7A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.235+7A>G
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18245
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.235+7A>G
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD

17-38073330-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073330
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073330
    reference: chr 17
allele count: 85
allele frequency: 7.003378100024718e-4
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.235+5G>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.235+5G>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.235+5G>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.235+5G>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2773+5G>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.235+5G>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.235+5G>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.235+5G>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.235+5G>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.66+5G>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.235+5G>C
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18246
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11886
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
hgvs: c.235+5G>C
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD

17-38073331-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073331
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073331
    reference: chr 17
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.235+4A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.235+4A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.235+4A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2773+4A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.235+4A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.235+4A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.235+4A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.235+4A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.235+4A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.66+4A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.235+4A>C
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.235+4A>C
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

17-38073332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073332
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073332
    reference: chr 17
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.235+3C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.235+3C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.235+3C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2773+3C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.235+3C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.235+3C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.235+3C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.235+3C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.235+3C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.235+3C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.66+3C>T
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15861
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.235+3C>T
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD

17-38073337-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073337
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073337
    reference: chr 17
allele count: 24
allele frequency: 1.977066034005536e-4
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.233A>G
  hgvsp: ENSP00000430157.1:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.233A>G
  hgvsp: ENSP00000429265.1:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.233A>G
  hgvsp: ENSP00000415049.1:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.233A>G
  hgvsp: ENSP00000377733.1:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.233A>G
  hgvsp: ENSP00000353465.3:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.233A>G
  hgvsp: ENSP00000312584.7:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.233A>G
  hgvsp: ENSP00000428712.1:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2771A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.233A>G
  hgvsp: ENSP00000377729.2:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.233A>G
  hgvsp: ENSP00000428217.1:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.64A>G
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln78Arg
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

17-38073344-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073344
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073344
    reference: chr 17
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.226G>A
  hgvsp: ENSP00000430157.1:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.57G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.226G>A
  hgvsp: ENSP00000429265.1:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.226G>A
  hgvsp: ENSP00000312584.7:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.226G>A
  hgvsp: ENSP00000428217.1:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.226G>A
  hgvsp: ENSP00000353465.3:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.226G>A
  hgvsp: ENSP00000377729.2:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.226G>A
  hgvsp: ENSP00000377733.1:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.226G>A
  hgvsp: ENSP00000428712.1:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.226G>A
  hgvsp: ENSP00000415049.1:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2764G>A
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly76Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/17-38073361-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073361
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073361
    reference: chr 17
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2747T>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.40T>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.209T>G
  hgvsp: ENSP00000428712.1:p.Leu70Ter
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.209T>G
  hgvsp: ENSP00000428217.1:p.Leu70Ter
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.209T>G
  hgvsp: ENSP00000312584.7:p.Leu70Ter
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.209T>G
  hgvsp: ENSP00000429265.1:p.Leu70Ter
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.209T>G
  hgvsp: ENSP00000430157.1:p.Leu70Ter
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.209T>G
  hgvsp: ENSP00000377733.1:p.Leu70Ter
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.209T>G
  hgvsp: ENSP00000377729.2:p.Leu70Ter
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.209T>G
  hgvsp: ENSP00000415049.1:p.Leu70Ter
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.209T>G
  hgvsp: ENSP00000353465.3:p.Leu70Ter
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu70Ter
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

17-38073367-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073367
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073367
    reference: chr 17
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.203A>G
  hgvsp: ENSP00000353465.3:p.Lys68Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.203A>G
  hgvsp: ENSP00000377729.2:p.Lys68Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.203A>G
  hgvsp: ENSP00000377733.1:p.Lys68Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.203A>G
  hgvsp: ENSP00000415049.1:p.Lys68Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.203A>G
  hgvsp: ENSP00000430157.1:p.Lys68Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.34A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.203A>G
  hgvsp: ENSP00000428712.1:p.Lys68Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.203A>G
  hgvsp: ENSP00000429265.1:p.Lys68Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2741A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.203A>G
  hgvsp: ENSP00000312584.7:p.Lys68Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.203A>G
  hgvsp: ENSP00000428217.1:p.Lys68Arg
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys68Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

17-38073376-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073376
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073376
    reference: chr 17
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.194A>G
  hgvsp: ENSP00000353465.3:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.194A>G
  hgvsp: ENSP00000415049.1:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.194A>G
  hgvsp: ENSP00000430157.1:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.194A>G
  hgvsp: ENSP00000377733.1:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.194A>G
  hgvsp: ENSP00000428217.1:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.25A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.194A>G
  hgvsp: ENSP00000312584.7:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.194A>G
  hgvsp: ENSP00000429265.1:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2732A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.194A>G
  hgvsp: ENSP00000377729.2:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.194A>G
  hgvsp: ENSP00000428712.1:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp65Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

17-38073379-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073379
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073379
    reference: chr 17
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.191C>T
  hgvsp: ENSP00000353465.3:p.Thr64Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.191C>T
  hgvsp: ENSP00000377733.1:p.Thr64Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.191C>T
  hgvsp: ENSP00000428217.1:p.Thr64Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.191C>T
  hgvsp: ENSP00000312584.7:p.Thr64Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2729C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.191C>T
  hgvsp: ENSP00000428712.1:p.Thr64Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.22C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.191C>T
  hgvsp: ENSP00000429265.1:p.Thr64Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.191C>T
  hgvsp: ENSP00000377729.2:p.Thr64Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.191C>T
  hgvsp: ENSP00000415049.1:p.Thr64Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.191C>T
  hgvsp: ENSP00000430157.1:p.Thr64Ile
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr64Ile
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

17-38073390-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073390
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073390
    reference: chr 17
allele count: 70
allele frequency: 5.765492702533522e-4
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.180C>A
  hgvsp: ENSP00000428217.1:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.180C>A
  hgvsp: ENSP00000429265.1:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.180C>A
  hgvsp: ENSP00000377733.1:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.180C>A
  hgvsp: ENSP00000415049.1:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.180C>A
  hgvsp: ENSP00000377729.2:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.180C>A
  hgvsp: ENSP00000312584.7:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.180C>A
  hgvsp: ENSP00000430157.1:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.180C>A
  hgvsp: ENSP00000428712.1:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.180C>A
  hgvsp: ENSP00000353465.3:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2718C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.11C>A
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp60Glu
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

17-38073397-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073397
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073397
    reference: chr 17
allele count: 5
allele frequency: 4.11820907323823e-5
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.173T>C
  hgvsp: ENSP00000377733.1:p.Leu58Pro
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2711T>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.173T>C
  hgvsp: ENSP00000377729.2:p.Leu58Pro
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.173T>C
  hgvsp: ENSP00000429265.1:p.Leu58Pro
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.173T>C
  hgvsp: ENSP00000428217.1:p.Leu58Pro
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.173T>C
  hgvsp: ENSP00000428712.1:p.Leu58Pro
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.173T>C
  hgvsp: ENSP00000430157.1:p.Leu58Pro
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.173T>C
  hgvsp: ENSP00000312584.7:p.Leu58Pro
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.173T>C
  hgvsp: ENSP00000353465.3:p.Leu58Pro
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.173T>C
  hgvsp: ENSP00000415049.1:p.Leu58Pro
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000464556
  gene symbol: GSDMB
  hgvsc: ENST00000464556.1:n.4T>C
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu58Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: A
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

17-38073406-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073406
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073406
    reference: chr 17
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.164G>A
  hgvsp: ENSP00000428712.1:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2702G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.164G>A
  hgvsp: ENSP00000377729.2:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.164G>A
  hgvsp: ENSP00000377733.1:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.164G>A
  hgvsp: ENSP00000353465.3:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.164G>A
  hgvsp: ENSP00000430157.1:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.164G>A
  hgvsp: ENSP00000429265.1:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.164G>A
  hgvsp: ENSP00000312584.7:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.164G>A
  hgvsp: ENSP00000415049.1:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.164G>A
  hgvsp: ENSP00000428217.1:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4412
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly55Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD

17-38073411-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073411
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073411
    reference: chr 17
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.159A>G
  hgvsp: ENST00000520542.1:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.159A>G
  hgvsp: ENST00000418519.1:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.159A>G
  hgvsp: ENST00000523371.1:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.159A>G
  hgvsp: ENST00000524039.1:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.159A>G
  hgvsp: ENST00000394175.2:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.159A>G
  hgvsp: ENST00000394179.1:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.159A>G
  hgvsp: ENST00000309481.7:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.159A>G
  hgvsp: ENST00000360317.3:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2697A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.159A>G
  hgvsp: ENST00000522564.1:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr53Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

17-38073412-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073412
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073412
    reference: chr 17
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2696C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.158C>A
  hgvsp: ENSP00000428217.1:p.Thr53Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.158C>A
  hgvsp: ENSP00000429265.1:p.Thr53Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.158C>A
  hgvsp: ENSP00000377733.1:p.Thr53Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.158C>A
  hgvsp: ENSP00000415049.1:p.Thr53Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.158C>A
  hgvsp: ENSP00000430157.1:p.Thr53Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.158C>A
  hgvsp: ENSP00000353465.3:p.Thr53Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.158C>A
  hgvsp: ENSP00000428712.1:p.Thr53Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.158C>A
  hgvsp: ENSP00000312584.7:p.Thr53Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.158C>A
  hgvsp: ENSP00000377729.2:p.Thr53Lys
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr53Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

17-38073417-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073417
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073417
    reference: chr 17
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.153C>T
  hgvsp: ENST00000524039.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.153C>T
  hgvsp: ENST00000523371.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.153C>T
  hgvsp: ENST00000520542.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.153C>T
  hgvsp: ENST00000360317.3:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.153C>T
  hgvsp: ENST00000522564.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.153C>T
  hgvsp: ENST00000394179.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.153C>T
  hgvsp: ENST00000309481.7:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2691C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.153C>T
  hgvsp: ENST00000394175.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.153C>T
  hgvsp: ENST00000418519.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His51His
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

17-38073420-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073420
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073420
    reference: chr 17
allele count: 8
allele frequency: 6.589134517181169e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2688G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.150G>A
  hgvsp: ENST00000394175.2:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.150G>A
  hgvsp: ENST00000394179.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.150G>A
  hgvsp: ENST00000524039.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.150G>A
  hgvsp: ENST00000360317.3:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.150G>A
  hgvsp: ENST00000520542.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.150G>A
  hgvsp: ENST00000522564.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.150G>A
  hgvsp: ENST00000309481.7:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.150G>A
  hgvsp: ENST00000418519.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.150G>A
  hgvsp: ENST00000523371.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg50Arg
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

17-38073421-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073421
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073421
    reference: chr 17
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.149G>A
  hgvsp: ENSP00000312584.7:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2687G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.149G>A
  hgvsp: ENSP00000429265.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.149G>A
  hgvsp: ENSP00000415049.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.149G>A
  hgvsp: ENSP00000428217.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.149G>A
  hgvsp: ENSP00000377729.2:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.149G>A
  hgvsp: ENSP00000353465.3:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.149G>A
  hgvsp: ENSP00000430157.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.149G>A
  hgvsp: ENSP00000377733.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.149G>A
  hgvsp: ENSP00000428712.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg50Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

17-38073430-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073430
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073430
    reference: chr 17
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.140T>C
  hgvsp: ENSP00000377733.1:p.Phe47Ser
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.140T>C
  hgvsp: ENSP00000428217.1:p.Phe47Ser
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.140T>C
  hgvsp: ENSP00000353465.3:p.Phe47Ser
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.140T>C
  hgvsp: ENSP00000429265.1:p.Phe47Ser
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.140T>C
  hgvsp: ENSP00000377729.2:p.Phe47Ser
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.140T>C
  hgvsp: ENSP00000312584.7:p.Phe47Ser
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.140T>C
  hgvsp: ENSP00000428712.1:p.Phe47Ser
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.140T>C
  hgvsp: ENSP00000415049.1:p.Phe47Ser
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2678T>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.140T>C
  hgvsp: ENSP00000430157.1:p.Phe47Ser
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Phe47Ser
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

17-38073432-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073432
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073432
    reference: chr 17
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2676C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.138C>A
  hgvsp: ENSP00000415049.1:p.Phe46Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.138C>A
  hgvsp: ENSP00000312584.7:p.Phe46Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.138C>A
  hgvsp: ENSP00000377733.1:p.Phe46Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.138C>A
  hgvsp: ENSP00000428712.1:p.Phe46Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.138C>A
  hgvsp: ENSP00000353465.3:p.Phe46Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.138C>A
  hgvsp: ENSP00000428217.1:p.Phe46Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.138C>A
  hgvsp: ENSP00000377729.2:p.Phe46Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.138C>A
  hgvsp: ENSP00000429265.1:p.Phe46Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.138C>A
  hgvsp: ENSP00000430157.1:p.Phe46Leu
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8415
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Phe46Leu
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-38073448-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073448
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073448
    reference: chr 17
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.122G>A
  hgvsp: ENSP00000312584.7:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.122G>A
  hgvsp: ENSP00000429265.1:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.122G>A
  hgvsp: ENSP00000430157.1:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.122G>A
  hgvsp: ENSP00000428217.1:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.122G>A
  hgvsp: ENSP00000428712.1:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2660G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.122G>A
  hgvsp: ENSP00000415049.1:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.122G>A
  hgvsp: ENSP00000377729.2:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.122G>A
  hgvsp: ENSP00000377733.1:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.122G>A
  hgvsp: ENSP00000353465.3:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly41Glu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-38073450-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073450
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073450
    reference: chr 17
allele count: 6
allele frequency: 4.941850887885876e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.120G>A
  hgvsp: ENST00000360317.3:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.120G>A
  hgvsp: ENST00000523371.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2658G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.120G>A
  hgvsp: ENST00000309481.7:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.120G>A
  hgvsp: ENST00000418519.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.120G>A
  hgvsp: ENST00000394179.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.120G>A
  hgvsp: ENST00000524039.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.120G>A
  hgvsp: ENST00000394175.2:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.120G>A
  hgvsp: ENST00000520542.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.120G>A
  hgvsp: ENST00000522564.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11915
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val40Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

17-38073457-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073457
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073456
    reference: chr 17
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.112delC
  hgvsp: ENSP00000353465.3:p.His38IlefsTer21
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.112delC
  hgvsp: ENSP00000377729.2:p.His38IlefsTer21
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.112delC
  hgvsp: ENSP00000428217.1:p.His38IlefsTer21
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.112delC
  hgvsp: ENSP00000377733.1:p.His38IlefsTer21
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.112delC
  hgvsp: ENSP00000415049.1:p.His38IlefsTer21
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2650delC
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.112delC
  hgvsp: ENSP00000312584.7:p.His38IlefsTer21
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.112delC
  hgvsp: ENSP00000428712.1:p.His38IlefsTer21
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.112delC
  hgvsp: ENSP00000429265.1:p.His38IlefsTer21
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.112delC
  hgvsp: ENSP00000430157.1:p.His38IlefsTer21
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3223
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His38IlefsTer21
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: TG
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-38073459-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073459
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073459
    reference: chr 17
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.111C>A
  hgvsp: ENSP00000353465.3:p.Phe37Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.111C>A
  hgvsp: ENSP00000377733.1:p.Phe37Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.111C>A
  hgvsp: ENSP00000430157.1:p.Phe37Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.111C>A
  hgvsp: ENSP00000428217.1:p.Phe37Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.111C>A
  hgvsp: ENSP00000428712.1:p.Phe37Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.111C>A
  hgvsp: ENSP00000415049.1:p.Phe37Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.111C>A
  hgvsp: ENSP00000312584.7:p.Phe37Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2649C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.111C>A
  hgvsp: ENSP00000429265.1:p.Phe37Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.111C>A
  hgvsp: ENSP00000377729.2:p.Phe37Leu
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4413
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe37Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-38073461-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073461
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073461
    reference: chr 17
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.109T>G
  hgvsp: ENSP00000377729.2:p.Phe37Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.109T>G
  hgvsp: ENSP00000377733.1:p.Phe37Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.109T>G
  hgvsp: ENSP00000429265.1:p.Phe37Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.109T>G
  hgvsp: ENSP00000428217.1:p.Phe37Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.109T>G
  hgvsp: ENSP00000415049.1:p.Phe37Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.109T>G
  hgvsp: ENSP00000353465.3:p.Phe37Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.109T>G
  hgvsp: ENSP00000428712.1:p.Phe37Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.109T>G
  hgvsp: ENSP00000430157.1:p.Phe37Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.109T>G
  hgvsp: ENSP00000312584.7:p.Phe37Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2647T>G
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29393
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Phe37Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

17-38073466-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073466
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073466
    reference: chr 17
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.104G>A
  hgvsp: ENSP00000430157.1:p.Arg35His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.104G>A
  hgvsp: ENSP00000377729.2:p.Arg35His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.104G>A
  hgvsp: ENSP00000377733.1:p.Arg35His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.104G>A
  hgvsp: ENSP00000429265.1:p.Arg35His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.104G>A
  hgvsp: ENSP00000428712.1:p.Arg35His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.104G>A
  hgvsp: ENSP00000428217.1:p.Arg35His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.104G>A
  hgvsp: ENSP00000312584.7:p.Arg35His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.104G>A
  hgvsp: ENSP00000353465.3:p.Arg35His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2642G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.104G>A
  hgvsp: ENSP00000415049.1:p.Arg35His
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg35His
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

17-38073467-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073467
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073467
    reference: chr 17
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.103C>T
  hgvsp: ENSP00000428712.1:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.103C>T
  hgvsp: ENSP00000428217.1:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.103C>T
  hgvsp: ENSP00000377733.1:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.103C>T
  hgvsp: ENSP00000353465.3:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.103C>T
  hgvsp: ENSP00000429265.1:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.103C>T
  hgvsp: ENSP00000312584.7:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2641C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.103C>T
  hgvsp: ENSP00000377729.2:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.103C>T
  hgvsp: ENSP00000430157.1:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.103C>T
  hgvsp: ENSP00000415049.1:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg35Cys
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

17-38073480-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073480
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073480
    reference: chr 17
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.90T>C
  hgvsp: ENST00000418519.1:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.90T>C
  hgvsp: ENST00000524039.1:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.90T>C
  hgvsp: ENST00000394179.1:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2628T>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.90T>C
  hgvsp: ENST00000522564.1:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.90T>C
  hgvsp: ENST00000309481.7:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.90T>C
  hgvsp: ENST00000520542.1:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.90T>C
  hgvsp: ENST00000394175.2:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.90T>C
  hgvsp: ENST00000360317.3:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.90T>C
  hgvsp: ENST00000523371.1:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp30Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP

17-38073481-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073481
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073481
    reference: chr 17
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.89A>G
  hgvsp: ENSP00000429265.1:p.Asp30Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.89A>G
  hgvsp: ENSP00000353465.3:p.Asp30Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.89A>G
  hgvsp: ENSP00000430157.1:p.Asp30Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.89A>G
  hgvsp: ENSP00000415049.1:p.Asp30Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2627A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.89A>G
  hgvsp: ENSP00000377733.1:p.Asp30Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.89A>G
  hgvsp: ENSP00000377729.2:p.Asp30Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.89A>G
  hgvsp: ENSP00000428712.1:p.Asp30Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.89A>G
  hgvsp: ENSP00000312584.7:p.Asp30Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.89A>G
  hgvsp: ENSP00000428217.1:p.Asp30Gly
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp30Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/17-38073483-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073483
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073483
    reference: chr 17
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.87T>G
  hgvsp: ENST00000520542.1:c.87T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.87T>G
  hgvsp: ENST00000394175.2:c.87T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2625T>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.87T>G
  hgvsp: ENST00000394179.1:c.87T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.87T>G
  hgvsp: ENST00000522564.1:c.87T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.87T>G
  hgvsp: ENST00000523371.1:c.87T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.87T>G
  hgvsp: ENST00000524039.1:c.87T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.87T>G
  hgvsp: ENST00000309481.7:c.87T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.87T>G
  hgvsp: ENST00000418519.1:c.87T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.87T>G
  hgvsp: ENST00000360317.3:c.87T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val29Val
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/17-38073487-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073487
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073487
    reference: chr 17
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.83T>G
  hgvsp: ENSP00000415049.1:p.Leu28Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.83T>G
  hgvsp: ENSP00000353465.3:p.Leu28Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.83T>G
  hgvsp: ENSP00000429265.1:p.Leu28Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.83T>G
  hgvsp: ENSP00000430157.1:p.Leu28Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.83T>G
  hgvsp: ENSP00000428217.1:p.Leu28Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.83T>G
  hgvsp: ENSP00000377733.1:p.Leu28Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.83T>G
  hgvsp: ENSP00000312584.7:p.Leu28Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2621T>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.83T>G
  hgvsp: ENSP00000377729.2:p.Leu28Arg
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.83T>G
  hgvsp: ENSP00000428712.1:p.Leu28Arg
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu28Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

17-38073490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073490
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073490
    reference: chr 17
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.80G>A
  hgvsp: ENSP00000353465.3:p.Ser27Asn
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.80G>A
  hgvsp: ENSP00000428712.1:p.Ser27Asn
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.80G>A
  hgvsp: ENSP00000428217.1:p.Ser27Asn
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2618G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.80G>A
  hgvsp: ENSP00000430157.1:p.Ser27Asn
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.80G>A
  hgvsp: ENSP00000377729.2:p.Ser27Asn
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.80G>A
  hgvsp: ENSP00000429265.1:p.Ser27Asn
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.80G>A
  hgvsp: ENSP00000377733.1:p.Ser27Asn
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.80G>A
  hgvsp: ENSP00000312584.7:p.Ser27Asn
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.80G>A
  hgvsp: ENSP00000415049.1:p.Ser27Asn
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29404
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser27Asn
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

17-38073491-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073491
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073491
    reference: chr 17
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.79A>G
  hgvsp: ENSP00000430157.1:p.Ser27Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.79A>G
  hgvsp: ENSP00000377729.2:p.Ser27Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.79A>G
  hgvsp: ENSP00000429265.1:p.Ser27Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.79A>G
  hgvsp: ENSP00000353465.3:p.Ser27Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.79A>G
  hgvsp: ENSP00000377733.1:p.Ser27Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.79A>G
  hgvsp: ENSP00000312584.7:p.Ser27Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.79A>G
  hgvsp: ENSP00000428217.1:p.Ser27Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2617A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.79A>G
  hgvsp: ENSP00000415049.1:p.Ser27Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.79A>G
  hgvsp: ENSP00000428712.1:p.Ser27Gly
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser27Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

17-38073494-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073494
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073494
    reference: chr 17
allele count: 7
allele frequency: 5.765682656826568e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.76A>G
  hgvsp: ENSP00000428712.1:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2614A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.76A>G
  hgvsp: ENSP00000353465.3:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.76A>G
  hgvsp: ENSP00000312584.7:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.76A>G
  hgvsp: ENSP00000377733.1:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.76A>G
  hgvsp: ENSP00000428217.1:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.76A>G
  hgvsp: ENSP00000430157.1:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.76A>G
  hgvsp: ENSP00000429265.1:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.76A>G
  hgvsp: ENSP00000415049.1:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.76A>G
  hgvsp: ENSP00000377729.2:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg26Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

17-38073497-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073497
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073497
    reference: chr 17
allele count: 5
allele frequency: 4.118412599047823e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.73G>A
  hgvsp: ENSP00000377729.2:p.Val25Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.73G>A
  hgvsp: ENSP00000353465.3:p.Val25Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.73G>A
  hgvsp: ENSP00000377733.1:p.Val25Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2611G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.73G>A
  hgvsp: ENSP00000430157.1:p.Val25Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.73G>A
  hgvsp: ENSP00000415049.1:p.Val25Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.73G>A
  hgvsp: ENSP00000312584.7:p.Val25Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.73G>A
  hgvsp: ENSP00000428217.1:p.Val25Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.73G>A
  hgvsp: ENSP00000429265.1:p.Val25Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.73G>A
  hgvsp: ENSP00000428712.1:p.Val25Ile
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18359
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val25Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

17-38073498-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073498
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073498
    reference: chr 17
allele count: 32
allele frequency: 2.635697224281361e-4
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.72C>T
  hgvsp: ENST00000523371.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.72C>T
  hgvsp: ENST00000418519.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.72C>T
  hgvsp: ENST00000524039.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.72C>T
  hgvsp: ENST00000309481.7:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.72C>T
  hgvsp: ENST00000394179.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.72C>T
  hgvsp: ENST00000520542.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.72C>T
  hgvsp: ENST00000394175.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.72C>T
  hgvsp: ENST00000360317.3:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.72C>T
  hgvsp: ENST00000522564.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2610C>T
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4407
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala24Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

17-38073499-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073499
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073499
    reference: chr 17
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.71C>T
  hgvsp: ENSP00000428712.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2609C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.71C>T
  hgvsp: ENSP00000415049.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.71C>T
  hgvsp: ENSP00000429265.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.71C>T
  hgvsp: ENSP00000377729.2:p.Ala24Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.71C>T
  hgvsp: ENSP00000312584.7:p.Ala24Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.71C>T
  hgvsp: ENSP00000377733.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.71C>T
  hgvsp: ENSP00000428217.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.71C>T
  hgvsp: ENSP00000430157.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.71C>T
  hgvsp: ENSP00000353465.3:p.Ala24Val
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala24Val
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

17-38073510-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073510
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073510
    reference: chr 17
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.60G>A
  hgvsp: ENST00000418519.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.60G>A
  hgvsp: ENST00000523371.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.60G>A
  hgvsp: ENST00000524039.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.60G>A
  hgvsp: ENST00000522564.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.60G>A
  hgvsp: ENST00000309481.7:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.60G>A
  hgvsp: ENST00000520542.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.60G>A
  hgvsp: ENST00000394175.2:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.60G>A
  hgvsp: ENST00000394179.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2598G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.60G>A
  hgvsp: ENST00000360317.3:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly20Gly
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

17-38073514-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073514
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073514
    reference: chr 17
allele count: 4
allele frequency: 3.294675803900896e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.56G>A
  hgvsp: ENSP00000428712.1:p.Gly19Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.56G>A
  hgvsp: ENSP00000353465.3:p.Gly19Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2594G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.56G>A
  hgvsp: ENSP00000377733.1:p.Gly19Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.56G>A
  hgvsp: ENSP00000415049.1:p.Gly19Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.56G>A
  hgvsp: ENSP00000428217.1:p.Gly19Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.56G>A
  hgvsp: ENSP00000429265.1:p.Gly19Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.56G>A
  hgvsp: ENSP00000430157.1:p.Gly19Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.56G>A
  hgvsp: ENSP00000312584.7:p.Gly19Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.56G>A
  hgvsp: ENSP00000377729.2:p.Gly19Glu
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29419
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly19Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

17-38073518-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073518
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073518
    reference: chr 17
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.52G>A
  hgvsp: ENSP00000353465.3:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.52G>A
  hgvsp: ENSP00000312584.7:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.52G>A
  hgvsp: ENSP00000428712.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.52G>A
  hgvsp: ENSP00000377733.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.52G>A
  hgvsp: ENSP00000429265.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.52G>A
  hgvsp: ENSP00000428217.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.52G>A
  hgvsp: ENSP00000430157.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.52G>A
  hgvsp: ENSP00000415049.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.52G>A
  hgvsp: ENSP00000377729.2:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2590G>A
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala18Thr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

17-38073521-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073521
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073521
    reference: chr 17
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.49G>C
  hgvsp: ENSP00000428217.1:p.Asp17His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.49G>C
  hgvsp: ENSP00000430157.1:p.Asp17His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.49G>C
  hgvsp: ENSP00000377733.1:p.Asp17His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2587G>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.49G>C
  hgvsp: ENSP00000312584.7:p.Asp17His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.49G>C
  hgvsp: ENSP00000377729.2:p.Asp17His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.49G>C
  hgvsp: ENSP00000429265.1:p.Asp17His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.49G>C
  hgvsp: ENSP00000353465.3:p.Asp17His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.49G>C
  hgvsp: ENSP00000415049.1:p.Asp17His
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.49G>C
  hgvsp: ENSP00000428712.1:p.Asp17His
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3219
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp17His
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-38073527-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073527
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073527
    reference: chr 17
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.43G>C
  hgvsp: ENSP00000415049.1:p.Glu15Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.43G>C
  hgvsp: ENSP00000428217.1:p.Glu15Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.43G>C
  hgvsp: ENSP00000312584.7:p.Glu15Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.43G>C
  hgvsp: ENSP00000377733.1:p.Glu15Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.43G>C
  hgvsp: ENSP00000430157.1:p.Glu15Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.43G>C
  hgvsp: ENSP00000353465.3:p.Glu15Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.43G>C
  hgvsp: ENSP00000428712.1:p.Glu15Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.43G>C
  hgvsp: ENSP00000377729.2:p.Glu15Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.43G>C
  hgvsp: ENSP00000429265.1:p.Glu15Gln
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2581G>C
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu15Gln
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

17-38073527-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073527
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073527
    reference: chr 17
allele count: 10
allele frequency: 8.236825198095645e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.43G>A
  hgvsp: ENSP00000428217.1:p.Glu15Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.43G>A
  hgvsp: ENSP00000415049.1:p.Glu15Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.43G>A
  hgvsp: ENSP00000377733.1:p.Glu15Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.43G>A
  hgvsp: ENSP00000353465.3:p.Glu15Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2581G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.43G>A
  hgvsp: ENSP00000429265.1:p.Glu15Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.43G>A
  hgvsp: ENSP00000312584.7:p.Glu15Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.43G>A
  hgvsp: ENSP00000377729.2:p.Glu15Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.43G>A
  hgvsp: ENSP00000430157.1:p.Glu15Lys
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.43G>A
  hgvsp: ENSP00000428712.1:p.Glu15Lys
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu15Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

17-38073530-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073530
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073530
    reference: chr 17
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.40A>G
  hgvsp: ENSP00000312584.7:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.40A>G
  hgvsp: ENSP00000415049.1:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.40A>G
  hgvsp: ENSP00000430157.1:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.40A>G
  hgvsp: ENSP00000377733.1:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.40A>G
  hgvsp: ENSP00000353465.3:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.40A>G
  hgvsp: ENSP00000428712.1:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.40A>G
  hgvsp: ENSP00000429265.1:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.40A>G
  hgvsp: ENSP00000428217.1:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2578A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.40A>G
  hgvsp: ENSP00000377729.2:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys14Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

17-38073533-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073533
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073533
    reference: chr 17
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.37G>A
  hgvsp: ENSP00000429265.1:p.Val13Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.37G>A
  hgvsp: ENSP00000353465.3:p.Val13Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.37G>A
  hgvsp: ENSP00000430157.1:p.Val13Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.37G>A
  hgvsp: ENSP00000312584.7:p.Val13Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.37G>A
  hgvsp: ENSP00000377729.2:p.Val13Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.37G>A
  hgvsp: ENSP00000428217.1:p.Val13Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.37G>A
  hgvsp: ENSP00000428712.1:p.Val13Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.37G>A
  hgvsp: ENSP00000415049.1:p.Val13Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.37G>A
  hgvsp: ENSP00000377733.1:p.Val13Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2575G>A
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val13Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/17-38073536-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073536
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073536
    reference: chr 17
allele count: 4
allele frequency: 3.294730079238259e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.34G>T
  hgvsp: ENSP00000377729.2:p.Val12Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.34G>T
  hgvsp: ENSP00000353465.3:p.Val12Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.34G>T
  hgvsp: ENSP00000430157.1:p.Val12Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.34G>T
  hgvsp: ENSP00000429265.1:p.Val12Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.34G>T
  hgvsp: ENSP00000312584.7:p.Val12Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.34G>T
  hgvsp: ENSP00000415049.1:p.Val12Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.34G>T
  hgvsp: ENSP00000428217.1:p.Val12Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.34G>T
  hgvsp: ENSP00000377733.1:p.Val12Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.34G>T
  hgvsp: ENSP00000428712.1:p.Val12Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2572G>T
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val12Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

17-38073539-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073539
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073539
    reference: chr 17
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.31A>T
  hgvsp: ENSP00000377733.1:p.Ile11Phe
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.31A>T
  hgvsp: ENSP00000429265.1:p.Ile11Phe
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.31A>T
  hgvsp: ENSP00000415049.1:p.Ile11Phe
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.31A>T
  hgvsp: ENSP00000377729.2:p.Ile11Phe
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.31A>T
  hgvsp: ENSP00000430157.1:p.Ile11Phe
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.31A>T
  hgvsp: ENSP00000312584.7:p.Ile11Phe
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.31A>T
  hgvsp: ENSP00000353465.3:p.Ile11Phe
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.31A>T
  hgvsp: ENSP00000428712.1:p.Ile11Phe
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.31A>T
  hgvsp: ENSP00000428217.1:p.Ile11Phe
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2569A>T
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3218
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile11Phe
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

17-38073548-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073548
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073548
    reference: chr 17
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.22A>G
  hgvsp: ENSP00000428712.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.22A>G
  hgvsp: ENSP00000415049.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2560A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.22A>G
  hgvsp: ENSP00000377729.2:p.Ile8Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.22A>G
  hgvsp: ENSP00000377733.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.22A>G
  hgvsp: ENSP00000312584.7:p.Ile8Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.22A>G
  hgvsp: ENSP00000428217.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.22A>G
  hgvsp: ENSP00000430157.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.22A>G
  hgvsp: ENSP00000353465.3:p.Ile8Val
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.22A>G
  hgvsp: ENSP00000429265.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile8Val
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

17-38073559-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073559
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073559
    reference: chr 17
allele count: 4
allele frequency: 3.295653033648617e-5
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.11T>C
  hgvsp: ENSP00000377729.2:p.Val4Ala
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2549T>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.11T>C
  hgvsp: ENSP00000429265.1:p.Val4Ala
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.11T>C
  hgvsp: ENSP00000353465.3:p.Val4Ala
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.11T>C
  hgvsp: ENSP00000377733.1:p.Val4Ala
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.11T>C
  hgvsp: ENSP00000415049.1:p.Val4Ala
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.11T>C
  hgvsp: ENSP00000312584.7:p.Val4Ala
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.11T>C
  hgvsp: ENSP00000430157.1:p.Val4Ala
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.11T>C
  hgvsp: ENSP00000428712.1:p.Val4Ala
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.11T>C
  hgvsp: ENSP00000428217.1:p.Val4Ala
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val4Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

17-38073560-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073560
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073560
    reference: chr 17
allele count: 3
allele frequency: 2.471739775236463e-5
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.10G>A
  hgvsp: ENSP00000353465.3:p.Val4Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.10G>A
  hgvsp: ENSP00000428217.1:p.Val4Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.10G>A
  hgvsp: ENSP00000377733.1:p.Val4Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2548G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.10G>A
  hgvsp: ENSP00000415049.1:p.Val4Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.10G>A
  hgvsp: ENSP00000430157.1:p.Val4Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.10G>A
  hgvsp: ENSP00000312584.7:p.Val4Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.10G>A
  hgvsp: ENSP00000428712.1:p.Val4Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.10G>A
  hgvsp: ENSP00000377729.2:p.Val4Ile
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.10G>A
  hgvsp: ENSP00000429265.1:p.Val4Ile
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val4Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

17-38073561-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073561
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073561
    reference: chr 17
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.9C>T
  hgvsp: ENST00000520542.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.9C>T
  hgvsp: ENST00000418519.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2547C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.9C>T
  hgvsp: ENST00000309481.7:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.9C>T
  hgvsp: ENST00000394175.2:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.9C>T
  hgvsp: ENST00000394179.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.9C>T
  hgvsp: ENST00000360317.3:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.9C>T
  hgvsp: ENST00000524039.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.9C>T
  hgvsp: ENST00000523371.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.9C>T
  hgvsp: ENST00000522564.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8383
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser3Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

17-38073563-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073563
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073563
    reference: chr 17
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.7A>G
  hgvsp: ENSP00000430157.1:p.Ser3Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.7A>G
  hgvsp: ENSP00000428217.1:p.Ser3Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.7A>G
  hgvsp: ENSP00000353465.3:p.Ser3Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.7A>G
  hgvsp: ENSP00000312584.7:p.Ser3Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.7A>G
  hgvsp: ENSP00000377729.2:p.Ser3Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.7A>G
  hgvsp: ENSP00000415049.1:p.Ser3Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2545A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.7A>G
  hgvsp: ENSP00000377733.1:p.Ser3Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.7A>G
  hgvsp: ENSP00000429265.1:p.Ser3Gly
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.7A>G
  hgvsp: ENSP00000428712.1:p.Ser3Gly
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18336
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser3Gly
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

17-38073564-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073564
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073564
    reference: chr 17
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.6C>A
  hgvsp: ENSP00000377729.2:p.Phe2Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.6C>A
  hgvsp: ENSP00000353465.3:p.Phe2Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.6C>A
  hgvsp: ENSP00000430157.1:p.Phe2Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2544C>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.6C>A
  hgvsp: ENSP00000312584.7:p.Phe2Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.6C>A
  hgvsp: ENSP00000428712.1:p.Phe2Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.6C>A
  hgvsp: ENSP00000415049.1:p.Phe2Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.6C>A
  hgvsp: ENSP00000428217.1:p.Phe2Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.6C>A
  hgvsp: ENSP00000377733.1:p.Phe2Leu
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.6C>A
  hgvsp: ENSP00000429265.1:p.Phe2Leu
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe2Leu
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

17-38073567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073567
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073567
    reference: chr 17
allele count: 13
allele frequency: 1.071369704961266e-4
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.3G>A
  hgvsp: ENSP00000377733.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.3G>A
  hgvsp: ENSP00000312584.7:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.3G>A
  hgvsp: ENSP00000353465.3:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.3G>A
  hgvsp: ENSP00000377729.2:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.3G>A
  hgvsp: ENSP00000428217.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.3G>A
  hgvsp: ENSP00000415049.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2541G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.3G>A
  hgvsp: ENSP00000430157.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.3G>A
  hgvsp: ENSP00000428712.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.3G>A
  hgvsp: ENSP00000429265.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 29278
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

17-38073568-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073568
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073568
    reference: chr 17
allele count: 5
allele frequency: 4.120584793393878e-5
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.2T>C
  hgvsp: ENSP00000429265.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.2T>C
  hgvsp: ENSP00000428217.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.2T>C
  hgvsp: ENSP00000377733.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.2T>C
  hgvsp: ENSP00000430157.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.2T>C
  hgvsp: ENSP00000312584.7:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.2T>C
  hgvsp: ENSP00000353465.3:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.2T>C
  hgvsp: ENSP00000415049.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2540T>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.2T>C
  hgvsp: ENSP00000377729.2:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.2T>C
  hgvsp: ENSP00000428712.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

17-38073569-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073569
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073569
    reference: chr 17
allele count: 38
allele frequency: 3.131954174565235e-4
allele num: 121330
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.1A>G
  hgvsp: ENSP00000415049.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.1A>G
  hgvsp: ENSP00000377733.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.1A>G
  hgvsp: ENSP00000430157.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428712
  ensembl transcript: ENST00000524039
  gene symbol: GSDMB
  hgvsc: ENST00000524039.1:c.1A>G
  hgvsp: ENSP00000428712.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000428217
  ensembl transcript: ENST00000522564
  gene symbol: GSDMB
  hgvsc: ENST00000522564.1:c.1A>G
  hgvsp: ENSP00000428217.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.1A>G
  hgvsp: ENSP00000377729.2:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000353465
  ensembl transcript: ENST00000360317
  gene symbol: GSDMB
  hgvsc: ENST00000360317.3:c.1A>G
  hgvsp: ENSP00000353465.3:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.1A>G
  hgvsp: ENSP00000312584.7:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2539A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000429265
  ensembl transcript: ENST00000523371
  gene symbol: GSDMB
  hgvsc: ENST00000523371.1:c.1A>G
  hgvsp: ENSP00000429265.1:p.Met1?
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 29262
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 1
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-38073570-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073570
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073570
    reference: chr 17
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.-1A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.-1A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.-1A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2538A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.-1A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.-1A>G
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8371
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

17-38073572-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073572
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073572
    reference: chr 17
allele count: 6
allele frequency: 4.946087644673064e-5
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.-3G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.-3G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2536G>A
  variant of: http://identifiers.org/hgnc/23690
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8374
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29209
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4389
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3207
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 9.25e1
  variant carriers: 0
hgvs: c.-3G>A
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

17-38073573-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073573
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073573
    reference: chr 17
allele count: 4
allele frequency: 3.297609233305853e-5
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.-4C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2535C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.-4C>T
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/23690
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4388
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3253
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8506
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3204
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.25e1
  variant carriers: 0
hgvs: c.-4C>T
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

17-38073583-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073583
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073583
    reference: chr 17
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.-14T>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.-14T>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.-5-9T>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.-14T>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2525T>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.-14T>C
  variant of: http://identifiers.org/hgnc/23690
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3248
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2011
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4379
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3181
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
hgvs: c.-14T>C
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

17-38073612-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073612
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073612
    reference: chr 17
allele count: 2
allele frequency: 1.664696775482346e-5
allele num: 120142
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.-14-29A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.-43A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2496A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.-14-29A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.-14-29A>G
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.-5-38A>G
  variant of: http://identifiers.org/hgnc/23690
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14602
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5558
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6238
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4247
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3212
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2980
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2475
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

17-38073612-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38073612
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38073612
    reference: chr 17
allele count: 1
allele frequency: 8.323483877411729e-6
allele num: 120142
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000312584
  ensembl transcript: ENST00000309481
  gene symbol: GSDMB
  hgvsc: ENST00000309481.7:c.-14-29A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377729
  ensembl transcript: ENST00000394175
  gene symbol: GSDMB
  hgvsc: ENST00000394175.2:c.-43A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000377733
  ensembl transcript: ENST00000394179
  gene symbol: GSDMB
  hgvsc: ENST00000394179.1:c.-14-29A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000430157
  ensembl transcript: ENST00000520542
  gene symbol: GSDMB
  hgvsc: ENST00000520542.1:c.-5-38A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073605
  ensembl transcript: ENST00000477054
  gene symbol: GSDMB
  hgvsc: ENST00000477054.2:n.2496A>C
  variant of: http://identifiers.org/hgnc/23690
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073605
  ensembl protein: ENSP00000415049
  ensembl transcript: ENST00000418519
  gene symbol: GSDMB
  hgvsc: ENST00000418519.1:c.-14-29A>C
  variant of: http://identifiers.org/hgnc/23690
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14602
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 88
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4451
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2458
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6418
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1003
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3096
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12409
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2609
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2725
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5294
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3646
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6109
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4206
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519756838905775e-5
allele num: 65800
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

VQSLOD
type: SiteQuality
SIO_000300: 6.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.796e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.435e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.718539e6

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8445
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 1561
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 996
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7993
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3251
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22642
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3124
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4365
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1338
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-5
allele num: 66120
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.744896178677369e-4
allele num: 11462
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.391e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.894637e6

VQSLOD
type: SiteQuality
SIO_000300: 1.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

QD
type: SiteQuality
SIO_000300: 1.398e1

GenotypeQuality
all individuals: 1299
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8444
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 711
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3132
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8067
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4368
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23216
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.147792942333702e-5
allele num: 16266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.746e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.117e0

VQSLOD
type: SiteQuality
SIO_000300: -1.881e0

MQRankSum
type: SiteQuality
SIO_000300: 5.93e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.832e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

DP
type: SiteQuality
SIO_000300: 1.898057e6

GenotypeQuality
all individuals: 765
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.700191404210893e-5
allele num: 11494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66224
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.855050115651503e-4
allele num: 10376
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.46e-1

FS
type: SiteQuality
SIO_000300: 2.769e0

QD
type: SiteQuality
SIO_000300: 1.521e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.439e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 1.919326e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 2026
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 4407
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16767865483419e-4
allele num: 8564
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.875e-1

MQ
type: SiteQuality
SIO_000300: 5.405e1

QD
type: SiteQuality
SIO_000300: 2.96e0

MQRankSum
type: SiteQuality
SIO_000300: -4.966e0

DP
type: SiteQuality
SIO_000300: 1.950782e6

FS
type: SiteQuality
SIO_000300: 1.128e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.274e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2029
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.99847026005579e-5
allele num: 66678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

DP
type: SiteQuality
SIO_000300: 1.959161e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.19e-1

QD
type: SiteQuality
SIO_000300: 1.105e1

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

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

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 8505
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variant carriers: 0

GenotypeQuality
all individuals: 8447
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.424242424242424e-4
allele num: 16500
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: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.705e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 3.775e0

VQSLOD
type: SiteQuality
SIO_000300: 9.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

QD
type: SiteQuality
SIO_000300: 1.173e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

DP
type: SiteQuality
SIO_000300: 1.96024e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-2

GenotypeDepth
all individuals: 235
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variant carriers: 0

GenotypeDepth
all individuals: 1040
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variant carriers: 0

GenotypeQuality
all individuals: 1451
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 6610
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.97e-2

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.960743e6

FS
type: SiteQuality
SIO_000300: 1.1803e1

QD
type: SiteQuality
SIO_000300: 1.804e1

GenotypeDepth
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variant carriers: 10

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 85

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3270
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.91323885240235e-4
allele num: 11572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.05143721633888e-4
allele num: 6610
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 8.094495742894831e-4
allele num: 66712
num of homozygotes: 0

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

South Asian
type: Population
allele count: 15
allele frequency: 9.085402786190188e-4
allele num: 16510
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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DP
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FS
type: SiteQuality
SIO_000300: 7.51e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.499e1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 29310
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
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
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.299e1

VQSLOD
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DP
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ClippingRankSum
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SIO_000300: 2.5e-1

InbreedingCoeff
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SIO_000300: 1.84e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.1e-2

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

FS
type: SiteQuality
SIO_000300: 1.1823e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 3228
bin: 7.25e1
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: 6612
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997691777331455e-5
allele num: 66718
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

InbreedingCoeff
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SIO_000300: 1.47e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.63e-1

VQSLOD
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DP
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SIO_000300: 1.961258e6

BaseQRankSum
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ClippingRankSum
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SIO_000300: -6.67e-1

MQ
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SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 7.103e0

QD
type: SiteQuality
SIO_000300: 1.304e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 24

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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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 (Non-Finnish)
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allele count: 22
allele frequency: 3.296966790552691e-4
allele num: 66728
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 4.02e0

ClippingRankSum
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SIO_000300: -1.52e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
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SIO_000300: 1.96281e6

FS
type: SiteQuality
SIO_000300: 2.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

QD
type: SiteQuality
SIO_000300: 1.335e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

East Asian
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allele count: 0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.279e1

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.786e0

FS
type: SiteQuality
SIO_000300: 8.885e0

DP
type: SiteQuality
SIO_000300: 1.96168e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

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

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

Other
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allele frequency: 0.0e0
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Latino
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 1
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allele num: 10406
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VQSLOD
type: SiteQuality
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ClippingRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQ
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

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

East Asian
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Latino
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South Asian
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European (Non-Finnish)
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num of homozygotes: 0

Other
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European (Finnish)
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FS
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QD
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ClippingRankSum
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DP
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BaseQRankSum
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VQSLOD
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MQ
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

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

East Asian
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num of homozygotes: 0

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

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

African
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 66740
num of homozygotes: 0

Other
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VQSLOD
type: SiteQuality
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DP
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BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 7.69e-1

QD
type: SiteQuality
SIO_000300: 1.265e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

GenotypeDepth
all individuals: 275
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5673
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4408
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8477
bin: 9.75e1
variant carriers: 70

GenotypeQuality
all individuals: 2016
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 26
allele frequency: 1.574612403100775e-3
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 40
allele frequency: 5.993407252022775e-4
allele num: 66740
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: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.79e0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

ReadPosRankSum
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SIO_000300: 5.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.05e0

DP
type: SiteQuality
SIO_000300: 1.96943e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.27e-2

GenotypeDepth
all individuals: 168
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 5

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29385
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1445
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.491759065028469e-5
allele num: 66740
num of homozygotes: 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

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

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

DP
type: SiteQuality
SIO_000300: 1.962565e6

FS
type: SiteQuality
SIO_000300: 1.4436e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.298e0

VQSLOD
type: SiteQuality
SIO_000300: -2.065e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

QD
type: SiteQuality
SIO_000300: 1.36e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 29386
bin: 6.25e1
variant carriers: 0

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

African
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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 (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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

FS
type: SiteQuality
SIO_000300: 2.398e0

DP
type: SiteQuality
SIO_000300: 1.96203e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.065e0

ReadPosRankSum
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SIO_000300: 1.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.465e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

MQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

QD
type: SiteQuality
SIO_000300: 1.528e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e0

FS
type: SiteQuality
SIO_000300: 2.916e0

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 1.961976e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.255e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 4410
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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

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

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

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

QD
type: SiteQuality
SIO_000300: 4.6e-1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.44e-1

InbreedingCoeff
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VQSLOD
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FS
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.297e0

QD
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -7.997e-1

GenotypeQuality
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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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allele count: 8
allele frequency: 4.844961240310077e-4
allele num: 16512
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.67e-1

VQSLOD
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InbreedingCoeff
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FS
type: SiteQuality
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ReadPosRankSum
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DP
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BaseQRankSum
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MQRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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East Asian
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African
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European (Non-Finnish)
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Other
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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QD
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FS
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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MQ
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ClippingRankSum
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DP
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Latino
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DP
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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QD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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European (Finnish)
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African
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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QD
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DP
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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Other
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African
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ClippingRankSum
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DP
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FS
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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Latino
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Other
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East Asian
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FS
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VQSLOD
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MQ
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MQRankSum
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BaseQRankSum
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QD
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DP
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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African
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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FS
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DP
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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East Asian
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African
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FS
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.96209e6

GenotypeQuality
all individuals: 29395
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4413
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
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: 66740
num of homozygotes: 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

FS
type: SiteQuality
SIO_000300: 3.857e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.96e-1

QD
type: SiteQuality
SIO_000300: 9.8e-1

DP
type: SiteQuality
SIO_000300: 1.96194e6

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
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

DP
type: SiteQuality
SIO_000300: 1.962299e6

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

QD
type: SiteQuality
SIO_000300: 1.479e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 29398
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variant carriers: 0

GenotypeQuality
all individuals: 4411
bin: 7.75e1
variant carriers: 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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
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: 10404
num of homozygotes: 0

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

South Asian
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allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.24e-1

QD
type: SiteQuality
SIO_000300: 9.050000000000001e0

DP
type: SiteQuality
SIO_000300: 1.962484e6

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

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8539
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.372e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.48e0

FS
type: SiteQuality
SIO_000300: 1.0866e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

VQSLOD
type: SiteQuality
SIO_000300: -1.256e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

DP
type: SiteQuality
SIO_000300: 1.962011e6

GenotypeQuality
all individuals: 1445
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8409
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.08e-1

DP
type: SiteQuality
SIO_000300: 1.961943e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.35e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 7.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.251e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 1.271e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 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
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.12e-1

MQ
type: SiteQuality
SIO_000300: 5.921e1

DP
type: SiteQuality
SIO_000300: 1.962376e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

FS
type: SiteQuality
SIO_000300: 1.131e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.961888e6

ReadPosRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
SIO_000300: 1.197e1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.712e0

VQSLOD
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SIO_000300: 1.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.66e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66738
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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ReadPosRankSum
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SIO_000300: 1.34e0

BaseQRankSum
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VQSLOD
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QD
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GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

African
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Latino
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Other
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East Asian
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QD
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 5.993766482857828e-5
allele num: 66736
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South Asian
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Latino
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African
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BaseQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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FS
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

African
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allele count: 27
allele frequency: 2.594656928694984e-3
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

South Asian
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allele frequency: 1.211240310077519e-4
allele num: 16512
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Other
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East Asian
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allele num: 8654
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InbreedingCoeff
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QD
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FS
type: SiteQuality
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.93e-1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
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allele num: 908
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

European (Finnish)
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South Asian
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ReadPosRankSum
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FS
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 908
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele num: 66734
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African
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East Asian
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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num of homozygotes: 0

South Asian
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Other
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East Asian
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African
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European (Non-Finnish)
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Latino
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66736
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European (Finnish)
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allele num: 6614
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South Asian
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African
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Latino
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
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)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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MQ
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FS
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QD
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SIO_000300: 1.7e1

VQSLOD
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DP
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

BaseQRankSum
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SIO_000300: 2.04e0

GenotypeQuality
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variant carriers: 0

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

Other
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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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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BaseQRankSum
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VQSLOD
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FS
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SIO_000300: 1.288e0

QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.5e-2

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.48e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 7
allele frequency: 1.048940570024275e-4
allele num: 66734
num of homozygotes: 0

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

South Asian
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allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

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

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

MQRankSum
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SIO_000300: 9.3e-2

DP
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FS
type: SiteQuality
SIO_000300: 1.288e0

QD
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ClippingRankSum
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SIO_000300: 4.48e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
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SIO_000300: 1.0e-4

BaseQRankSum
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SIO_000300: -1.955e0

VQSLOD
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SIO_000300: 1.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.5e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
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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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.364e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: -7.37e-1

MQRankSum
type: SiteQuality
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DP
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SIO_000300: 1.961721e6

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.457e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Latino
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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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.296e0

ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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QD
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SIO_000300: 9.6e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

Other
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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

African
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allele count: 4
allele frequency: 3.843936190659235e-4
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: 4.99e-1

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

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 9.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.2e-1

DP
type: SiteQuality
SIO_000300: 1.960887e6

MQ
type: SiteQuality
SIO_000300: 5.915e1

FS
type: SiteQuality
SIO_000300: 2.7283e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.41e0

VQSLOD
type: SiteQuality
SIO_000300: -4.501e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.346e0

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29364
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2012
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3217
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8388
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1441
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4405
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.996282304970918e-5
allele num: 66708
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.363e0

QD
type: SiteQuality
SIO_000300: 1.574e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.36e0

DP
type: SiteQuality
SIO_000300: 1.960463e6

GenotypeQuality
all individuals: 29352
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2013
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8526
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4404
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3215
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
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

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.88e-1

QD
type: SiteQuality
SIO_000300: 1.448e1

DP
type: SiteQuality
SIO_000300: 1.960387e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.63e-1

FS
type: SiteQuality
SIO_000300: 4.616e0

VQSLOD
type: SiteQuality
SIO_000300: 8.080000000000001e-1

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3214
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4400
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8521
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29323
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 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: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
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 (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.229e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

QD
type: SiteQuality
SIO_000300: 1.095e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.959842e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

GenotypeQuality
all individuals: 29334
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4398
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8519
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2014
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8382
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3214
bin: 7.25e1
variant carriers: 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: 10402
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: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.814e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.941e0

QD
type: SiteQuality
SIO_000300: 1.059e1

DP
type: SiteQuality
SIO_000300: 1.959826e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.14e0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e-1

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3212
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8383
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29322
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 16506
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: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.739e0

FS
type: SiteQuality
SIO_000300: 5.965e0

MQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

DP
type: SiteQuality
SIO_000300: 1.959688e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

QD
type: SiteQuality
SIO_000300: 1.217e1

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8394
bin: 9.75e1
variant carriers: 13

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4395
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3208
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.270964614638875e-4
allele num: 16504
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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: 10396
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

DP
type: SiteQuality
SIO_000300: 1.959753e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.973e0

FS
type: SiteQuality
SIO_000300: 6.082e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3258
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8385
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variant carriers: 5

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4396
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29281
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3208
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 5
allele frequency: 4.809542131589073e-4
allele num: 10396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
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: 11576
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.604e0

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

DP
type: SiteQuality
SIO_000300: 1.959395e6

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 8.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-2

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

GenotypeQuality
all individuals: 118
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
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variant carriers: 0

GenotypeQuality
all individuals: 3209
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GenotypeQuality
all individuals: 8400
bin: 9.75e1
variant carriers: 37

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 3254
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variant carriers: 0

GenotypeQuality
all individuals: 8513
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4394
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1439
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.456619426201175e-4
allele num: 11572
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: 16504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

African
type: Population
allele count: 34
allele frequency: 3.270488649480569e-3
allele num: 10396
num of homozygotes: 1

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

VQSLOD
type: SiteQuality
SIO_000300: 5.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.55e0

QD
type: SiteQuality
SIO_000300: 1.632e1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

DP
type: SiteQuality
SIO_000300: 1.960789e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.79e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-1

GenotypeQuality
all individuals: 8519
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29260
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4396
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
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: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.738e0

QD
type: SiteQuality
SIO_000300: 1.378e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.783e0

MQRankSum
type: SiteQuality
SIO_000300: -3.35e-1

DP
type: SiteQuality
SIO_000300: 1.958773e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

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

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

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8504
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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: 3
allele frequency: 4.499100179964007e-5
allele num: 66680
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592464569650881e-4
allele num: 11572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.958813e6

MQRankSum
type: SiteQuality
SIO_000300: -1.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 6.053e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.61e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 9.210000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.14e-1

GenotypeQuality
all individuals: 2013
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 29189
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8374
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 42
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 4
allele frequency: 3.849114703618168e-4
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
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: 8642
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.86e-1

QD
type: SiteQuality
SIO_000300: 1.319e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.658e0

DP
type: SiteQuality
SIO_000300: 1.958297e6

MQRankSum
type: SiteQuality
SIO_000300: -1.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
all individuals: 1434
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28640
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8370
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8458
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502810255177181e-5
allele num: 66542
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.661e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.67e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: 4.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-2

DP
type: SiteQuality
SIO_000300: 1.951051e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e-1

GenotypeQuality
all individuals: 1219
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18707
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8360
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7234
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.370229912301493e-4
allele num: 8438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.95e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

DP
type: SiteQuality
SIO_000300: 1.86428e6

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.095e0

QD
type: SiteQuality
SIO_000300: 1.018e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.95e-1