5-150509136-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150509136
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150509136
    reference: chr 5
allele count: 1
allele frequency: 2.02249008979856e-5
allele num: 49444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-96T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+9103T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.700-46T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.796-46T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.205-7315T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-3129T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*225-46T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.386-46T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.796-46T>C
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11875
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7077
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1155
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5509
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9064
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17529
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

5-150510747-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510747
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510747
    reference: chr 5
allele count: 1
allele frequency: 8.315593400745077e-6
allele num: 120256
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7492T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*224+45T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.795+45T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8167T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.795+45T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.699+45T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4740T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1707T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.385+45T>C
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16973
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53133
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

5-150510752-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510752
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510752
    reference: chr 5
allele count: 131
allele frequency: 1.089089155664926e-3
allele num: 120284
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.795+40G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.795+40G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4745G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8162G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.699+40G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7487G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.385+40G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*224+40G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1712G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16989
  bin: 9.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4250
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 7.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

5-150510757-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510757
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510757
    reference: chr 5
allele count: 17324
allele frequency: 1.438822630477393e-1
allele num: 120404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7482G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*224+35G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8157G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.385+35G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1717G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.795+35G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4750G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.795+35G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.699+35G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.75e1
  variant carriers: 296
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 3.25e1
  variant carriers: 376
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 2.25e1
  variant carriers: 264
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 4.75e1
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 8.75e1
  variant carriers: 417
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 8.25e1
  variant carriers: 344
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 4.25e1
  variant carriers: 205
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 2.75e1
  variant carriers: 339
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 5.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 7.75e1
  variant carriers: 279
genotype depth: GenotypeDepth
  all individuals: 21213
  bin: 9.75e1
  variant carriers: 11839
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 6.75e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 6.25e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 9.25e1
  variant carriers: 521
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 5.75e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 7.25e1
  variant carriers: 223
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 6.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 2
num of homozygotes: 1381
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD

5-150510758-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510758
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510758
    reference: chr 5
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8156G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.699+34G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.795+34G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7481G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.385+34G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*224+34G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.795+34G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4751G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1718G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12859
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2319
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

5-150510779-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510779
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510779
    reference: chr 5
allele count: 4
allele frequency: 3.315210184325686e-5
allele num: 120656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8135G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4772G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*224+13G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.795+13G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1739G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.795+13G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.699+13G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7460G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.385+13G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12860
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/5-150510785-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510785
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510785
    reference: chr 5
allele count: 2
allele frequency: 1.65694591728526e-5
allele num: 120704
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.699+7G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.795+7G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8129G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.385+7G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*224+7G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4778G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1745G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7454G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.795+7G>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12858
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
hgvs: c.795+7G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

5-150510785-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510785
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510785
    reference: chr 5
allele count: 3
allele frequency: 2.48541887592789e-5
allele num: 120704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1745G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*224+7G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.385+7G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4778G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.795+7G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.699+7G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.795+7G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8129G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7454G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12858
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
hgvs: c.795+7G>A
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

5-150510787-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510787
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510787
    reference: chr 5
allele count: 3
allele frequency: 2.485171808211008e-5
allele num: 120716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.385+5G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.795+5G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8127G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7452G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.795+5G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.699+5G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1747G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*224+5G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4780G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12856
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 9.25e1
  variant carriers: 0
hgvs: c.795+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

5-150510788-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510788
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510788
    reference: chr 5
allele count: 4
allele frequency: 3.313342831582784e-5
allele num: 120724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7451C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*224+4C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1748C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.795+4C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.699+4C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.795+4C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4781C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.385+4C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8126C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12856
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52770
  bin: 9.75e1
  variant carriers: 4
hgvs: c.795+4C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

5-150510794-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510794
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510794
    reference: chr 5
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*222A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.793A>G
  hgvsp: ENSP00000346550.5:p.Lys265Glu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8120A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4787A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.793A>G
  hgvsp: ENSP00000348889.5:p.Lys265Glu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.383A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1754A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.697A>G
  hgvsp: ENSP00000430517.1:p.Lys233Glu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7445A>G
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12855
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys265Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

5-150510797-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510797
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510797
    reference: chr 5
allele count: 3
allele frequency: 2.484636663298604e-5
allele num: 120742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.694A>G
  hgvsp: ENSP00000430517.1:p.Met232Val
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*219A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7442A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4790A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.380A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8117A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.790A>G
  hgvsp: ENSP00000346550.5:p.Met264Val
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1757A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.790A>G
  hgvsp: ENSP00000348889.5:p.Met264Val
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12855
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52769
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met264Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

5-150510799-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510799
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510799
    reference: chr 5
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*217C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.788C>T
  hgvsp: ENSP00000346550.5:p.Ala263Val
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7440C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4792C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8115C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.692C>T
  hgvsp: ENSP00000430517.1:p.Ala231Val
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.788C>T
  hgvsp: ENSP00000348889.5:p.Ala263Val
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1759C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.378C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12856
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala263Val
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

5-150510799-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510799
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510799
    reference: chr 5
allele count: 2
allele frequency: 1.656424442199069e-5
allele num: 120742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.692C>A
  hgvsp: ENSP00000430517.1:p.Ala231Asp
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.378C>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8115C>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.788C>A
  hgvsp: ENSP00000346550.5:p.Ala263Asp
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4792C>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7440C>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1759C>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*217C>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.788C>A
  hgvsp: ENSP00000348889.5:p.Ala263Asp
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12856
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala263Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

5-150510807-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510807
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510807
    reference: chr 5
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1767C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.370C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8107C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7432C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.780C>T
  hgvsp: ENST00000356496.5:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4800C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*209C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.780C>T
  hgvsp: ENST00000354546.5:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.684C>T
  hgvsp: ENST00000523714.1:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12854
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu260Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

5-150510809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510809
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510809
    reference: chr 5
allele count: 2
allele frequency: 1.656314699792961e-5
allele num: 120750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8105C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.778C>T
  hgvsp: ENSP00000346550.5:p.Leu260Phe
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.778C>T
  hgvsp: ENSP00000348889.5:p.Leu260Phe
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4802C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.682C>T
  hgvsp: ENSP00000430517.1:p.Leu228Phe
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*207C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7430C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1769C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.368C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12854
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu260Phe
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

5-150510812-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510812
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510812
    reference: chr 5
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.775A>G
  hgvsp: ENSP00000348889.5:p.Arg259Gly
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4805A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7427A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.775A>G
  hgvsp: ENSP00000346550.5:p.Arg259Gly
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8102A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.679A>G
  hgvsp: ENSP00000430517.1:p.Arg227Gly
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*204A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.365A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1772A>G
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12853
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg259Gly
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

5-150510819-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510819
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510819
    reference: chr 5
allele count: 2
allele frequency: 1.656287266463495e-5
allele num: 120752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7420T>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.672T>A
  hgvsp: ENSP00000430517.1:p.Phe224Leu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.358T>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.768T>A
  hgvsp: ENSP00000348889.5:p.Phe256Leu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*197T>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.768T>A
  hgvsp: ENSP00000346550.5:p.Phe256Leu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4812T>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8095T>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1779T>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12853
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Phe256Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

5-150510828-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510828
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510828
    reference: chr 5
allele count: 5
allele frequency: 4.140581006326808e-5
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.349G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7411G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.663G>A
  hgvsp: ENST00000523714.1:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4821G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.759G>A
  hgvsp: ENST00000354546.5:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*188G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8086G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.759G>A
  hgvsp: ENST00000356496.5:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1788G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12854
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro253Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

5-150510829-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510829
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510829
    reference: chr 5
allele count: 5
allele frequency: 4.140581006326808e-5
allele num: 120756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7410C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.758C>T
  hgvsp: ENSP00000346550.5:p.Pro253Leu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8085C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*187C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.348C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.758C>T
  hgvsp: ENSP00000348889.5:p.Pro253Leu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.662C>T
  hgvsp: ENSP00000430517.1:p.Pro221Leu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4822C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1789C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12852
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro253Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

5-150510832-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510832
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510832
    reference: chr 5
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7407C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.755C>T
  hgvsp: ENSP00000346550.5:p.Thr252Ile
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.659C>T
  hgvsp: ENSP00000430517.1:p.Thr220Ile
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4825C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.755C>T
  hgvsp: ENSP00000348889.5:p.Thr252Ile
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.345C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8082C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*184C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1792C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12849
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr252Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

5-150510835-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510835
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510835
    reference: chr 5
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.752G>A
  hgvsp: ENSP00000346550.5:p.Ser251Asn
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.656G>A
  hgvsp: ENSP00000430517.1:p.Ser219Asn
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.342G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4828G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1795G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8079G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*181G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.752G>A
  hgvsp: ENSP00000348889.5:p.Ser251Asn
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7404G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12849
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser251Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

5-150510838-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510838
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510838
    reference: chr 5
allele count: 13
allele frequency: 1.07655106164497e-4
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.749G>A
  hgvsp: ENSP00000348889.5:p.Arg250Gln
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.339G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1798G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4831G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.749G>A
  hgvsp: ENSP00000346550.5:p.Arg250Gln
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.653G>A
  hgvsp: ENSP00000430517.1:p.Arg218Gln
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7401G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8076G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*178G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12852
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg250Gln
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

5-150510839-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510839
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510839
    reference: chr 5
allele count: 4
allele frequency: 3.312464805061446e-5
allele num: 120756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7400C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.338C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*177C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8075C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.652C>T
  hgvsp: ENSP00000430517.1:p.Arg218Trp
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1799C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.748C>T
  hgvsp: ENSP00000348889.5:p.Arg250Trp
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4832C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.748C>T
  hgvsp: ENSP00000346550.5:p.Arg250Trp
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12845
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52766
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg250Trp
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP

5-150510846-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510846
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510846
    reference: chr 5
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*170G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7393G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8068G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4839G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.741G>A
  hgvsp: ENST00000356496.5:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1806G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.645G>A
  hgvsp: ENST00000523714.1:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.741G>A
  hgvsp: ENST00000354546.5:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.331G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12842
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys247Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

5-150510852-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510852
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510852
    reference: chr 5
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4845A>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8062A>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.641-2A>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.327-2A>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.737-2A>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*166-2A>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1812A>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.737-2A>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7387A>C
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12842
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 9.25e1
  variant carriers: 0
hgvs: c.737-2A>C
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

5-150510856-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510856
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510856
    reference: chr 5
allele count: 2
allele frequency: 1.656891009709381e-5
allele num: 120708
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7383T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4849T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8058T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*166-6T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1816T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.737-6T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.641-6T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.327-6T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.737-6T>C
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12842
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 7.75e1
  variant carriers: 0
hgvs: c.737-6T>C
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

5-150510858-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510858
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510858
    reference: chr 5
allele count: 1
allele frequency: 8.284455048546906e-6
allele num: 120708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1818C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8056C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.327-8C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.641-8C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.737-8C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4851C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7381C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*166-8C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.737-8C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12841
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
hgvs: c.737-8C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

5-150510860-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510860
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510860
    reference: chr 5
allele count: 7
allele frequency: 5.799022450501201e-5
allele num: 120710
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4853C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.737-10C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.327-10C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8054C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7379C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1820C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*166-10C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.737-10C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.641-10C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12843
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3038
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
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: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

5-150510864-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510864
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510864
    reference: chr 5
allele count: 2
allele frequency: 1.656918463042434e-5
allele num: 120706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8050C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.327-14C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*166-14C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4857C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.737-14C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.737-14C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.641-14C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7375C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1824C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12839
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum

5-150510878-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510878
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510878
    reference: chr 5
allele count: 1
allele frequency: 8.285416010737898e-6
allele num: 120694
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7361A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*166-28A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8036A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1838A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.737-28A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4871A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.641-28A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.327-28A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.737-28A>G
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12837
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

5-150510882-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510882
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510882
    reference: chr 5
allele count: 6
allele frequency: 4.971414367387522e-5
allele num: 120690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.737-32G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4875G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8032G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.327-32G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7357G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*166-32G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.641-32G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1842G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.737-32G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12837
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

5-150510897-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510897
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510897
    reference: chr 5
allele count: 2
allele frequency: 1.657550140891762e-5
allele num: 120660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*166-47C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.327-47C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.737-47C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.737-47C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4890C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8017C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.641-47C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7342C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1857C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52760
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum

5-150510897-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510897
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510897
    reference: chr 5
allele count: 2
allele frequency: 1.657550140891762e-5
allele num: 120660
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.737-47C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.737-47C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.641-47C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4890C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8017C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*166-47C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.327-47C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1857C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7342C>G
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52760
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

5-150510898-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510898
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510898
    reference: chr 5
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.327-48C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1858C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4891C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*166-48C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.737-48C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8016C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7341C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.641-48C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.737-48C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52760
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

5-150510899-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150510899
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150510899
    reference: chr 5
allele count: 1
allele frequency: 8.289124668435012e-6
allele num: 120640
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-1859C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*166-49C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.327-49C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.737-49C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+8015C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.737-49C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.641-49C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-4892C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+7340C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

5-150511996-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150511996
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150511996
    reference: chr 5
allele count: 2
allele frequency: 3.734129947722181e-5
allele num: 53560
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.736+41C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-2956C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*165+41C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-5989C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6243C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6918C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.640+41C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.736+41C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.326+41C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15177
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20655
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3701
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

5-150512004-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512004
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512004
    reference: chr 5
allele count: 1
allele frequency: 1.804988989567164e-5
allele num: 55402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-5997A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*165+33A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.326+33A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.736+33A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-2964A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6910A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.736+33A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6235A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.640+33A>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6531
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5321
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4254
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

5-150512018-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512018
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512018
    reference: chr 5
allele count: 1
allele frequency: 1.578183195505334e-5
allele num: 63364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.736+19T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.640+19T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*165+19T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6011T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6221T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-2978T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6896T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.326+19T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.736+19T>C
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11480
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26768
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12675
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4520
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/5-150512024-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512024
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512024
    reference: chr 5
allele count: 1
allele frequency: 1.450578780933592e-5
allele num: 68938
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-2984G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.640+13G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.326+13G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.736+13G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6017G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6215G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.736+13G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6890G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*165+13G>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3701
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3732
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

5-150512024-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512024
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512024
    reference: chr 5
allele count: 3
allele frequency: 4.351736342800778e-5
allele num: 68938
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.736+13G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6890G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.736+13G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.326+13G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6017G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*165+13G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6215G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.640+13G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-2984G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17831
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

5-150512025-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512025
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512025
    reference: chr 5
allele count: 6
allele frequency: 8.476491862567812e-5
allele num: 70784
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.640+12C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6018C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6214C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.326+12C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.736+12C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.736+12C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6889C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*165+12C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-2985C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18267
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1735
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3472
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

5-150512027-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512027
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512027
    reference: chr 5
allele count: 1
allele frequency: 1.374192661811186e-5
allele num: 72770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-2987G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.736+10G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6020G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.326+10G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6887G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.736+10G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.640+10G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6212G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*165+10G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22933
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23127
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3256
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

5-150512040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512040
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512040
    reference: chr 5
allele count: 56
allele frequency: 6.600504467127131e-4
allele num: 84842
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.323G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6874G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.733G>A
  hgvsp: ENSP00000348889.5:p.Val245Ile
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6033G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6199G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.637G>A
  hgvsp: ENSP00000430517.1:p.Val213Ile
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*162G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.733G>A
  hgvsp: ENSP00000346550.5:p.Val245Ile
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3000G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5503
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4870
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26765
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17287
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2143
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2237
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val245Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

5-150512041-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512041
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512041
    reference: chr 5
allele count: 4
allele frequency: 4.626523861296815e-5
allele num: 86458
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*161C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.636C>T
  hgvsp: ENST00000523714.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.732C>T
  hgvsp: ENST00000356496.5:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6034C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6873C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.322C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3001C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.732C>T
  hgvsp: ENST00000354546.5:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6198C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27662
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2301
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala244Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

5-150512052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512052
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512052
    reference: chr 5
allele count: 1
allele frequency: 1.02992975879045e-5
allele num: 97094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.721C>T
  hgvsp: ENST00000356496.5:c.721C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6862C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.625C>T
  hgvsp: ENST00000523714.1:c.625C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6187C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*150C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.311C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.721C>T
  hgvsp: ENST00000354546.5:c.721C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3012C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6045C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33466
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu241Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP

5-150512055-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512055
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512055
    reference: chr 5
allele count: 1
allele frequency: 1.006542526421741e-5
allele num: 99350
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.718A>G
  hgvsp: ENSP00000346550.5:p.Lys240Glu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.622A>G
  hgvsp: ENSP00000430517.1:p.Lys208Glu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3015A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6048A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.308A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*147A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6184A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.718A>G
  hgvsp: ENSP00000348889.5:p.Lys240Glu
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6859A>G
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys240Glu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

5-150512059-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512059
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512059
    reference: chr 5
allele count: 1
allele frequency: 9.839614287119945e-6
allele num: 101630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.714T>C
  hgvsp: ENST00000356496.5:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.304T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6855T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6052T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.618T>C
  hgvsp: ENST00000523714.1:c.618T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.714T>C
  hgvsp: ENST00000354546.5:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*143T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3019T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6180T>C
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10038
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe238Phe
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD

5-150512081-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512081
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512081
    reference: chr 5
allele count: 1
allele frequency: 9.235657024640733e-6
allele num: 108276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.282G>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3041G>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.692G>C
  hgvsp: ENSP00000346550.5:p.Arg231Pro
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.596G>C
  hgvsp: ENSP00000430517.1:p.Arg199Pro
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6833G>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*121G>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.692G>C
  hgvsp: ENSP00000348889.5:p.Arg231Pro
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6158G>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6074G>C
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg231Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

5-150512081-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512081
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512081
    reference: chr 5
allele count: 7
allele frequency: 6.464959917248513e-5
allele num: 108276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6833G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.692G>A
  hgvsp: ENSP00000348889.5:p.Arg231Gln
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6158G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*121G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.596G>A
  hgvsp: ENSP00000430517.1:p.Arg199Gln
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.692G>A
  hgvsp: ENSP00000346550.5:p.Arg231Gln
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.282G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6074G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3041G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3405
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg231Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

5-150512087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512087
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512087
    reference: chr 5
allele count: 2
allele frequency: 1.836041494537776e-5
allele num: 108930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6080G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*115G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.686G>A
  hgvsp: ENSP00000348889.5:p.Ser229Asn
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.686G>A
  hgvsp: ENSP00000346550.5:p.Ser229Asn
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.276G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.590G>A
  hgvsp: ENSP00000430517.1:p.Ser197Asn
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6152G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6827G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3047G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37034
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser229Asn
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

5-150512095-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512095
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512095
    reference: chr 5
allele count: 1
allele frequency: 9.211665653383444e-6
allele num: 108558
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6088T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3055T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.678T>C
  hgvsp: ENST00000356496.5:c.678T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6819T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.582T>C
  hgvsp: ENST00000523714.1:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*107T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6144T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.678T>C
  hgvsp: ENST00000354546.5:c.678T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.268T>C
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7862
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile226Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

5-150512098-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512098
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512098
    reference: chr 5
allele count: 4
allele frequency: 3.69139904023625e-5
allele num: 108360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.579G>A
  hgvsp: ENST00000523714.1:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6816G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.675G>A
  hgvsp: ENST00000356496.5:c.675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*104G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3058G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.675G>A
  hgvsp: ENST00000354546.5:c.675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.265G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6091G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6141G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35493
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9619
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8054
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro225Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

5-150512100-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512100
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512100
    reference: chr 5
allele count: 2
allele frequency: 1.849659662622078e-5
allele num: 108128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6093C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.577C>T
  hgvsp: ENSP00000430517.1:p.Pro193Ser
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.673C>T
  hgvsp: ENSP00000348889.5:p.Pro225Ser
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6139C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.673C>T
  hgvsp: ENSP00000346550.5:p.Pro225Ser
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6814C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*102C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.263C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3060C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9530
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8372
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro225Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD

5-150512119-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512119
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512119
    reference: chr 5
allele count: 1
allele frequency: 9.588830929733047e-6
allele num: 104288
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.654T>C
  hgvsp: ENST00000354546.5:c.654T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.244T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6112T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.654T>C
  hgvsp: ENST00000356496.5:c.654T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6795T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.558T>C
  hgvsp: ENST00000523714.1:c.558T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3079T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6120T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*83T>C
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7204
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35248
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr218Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

5-150512127-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512127
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512127
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 101150
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.646G>A
  hgvsp: ENSP00000348889.5:p.Asp216Asn
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6787G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6112G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.550G>A
  hgvsp: ENSP00000430517.1:p.Asp184Asn
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3087G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.236G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*75G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6120G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.646G>A
  hgvsp: ENSP00000346550.5:p.Asp216Asn
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9318
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1779
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16355
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2675
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp216Asn
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: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

5-150512128-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512128
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512128
    reference: chr 5
allele count: 9
allele frequency: 8.8999644001424e-5
allele num: 101124
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.645C>T
  hgvsp: ENST00000354546.5:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6111C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6786C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.235C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.645C>T
  hgvsp: ENST00000356496.5:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.549C>T
  hgvsp: ENST00000523714.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3088C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*74C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6121C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10474
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25629
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2659
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe215Phe
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

5-150512132-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512132
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512132
    reference: chr 5
allele count: 1
allele frequency: 1.012453174040701e-5
allele num: 98770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545T>C
  hgvsp: ENSP00000430517.1:p.Val182Ala
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6125T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3092T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6782T>C
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641T>C
  hgvsp: ENSP00000346550.5:p.Val214Ala
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641T>C
  hgvsp: ENSP00000348889.5:p.Val214Ala
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6107T>C
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1384
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val214Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

5-150512136-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512136
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512136
    reference: chr 5
allele count: 137
allele frequency: 1.404235255529817e-3
allele num: 97562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-4G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6778G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-4G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-4G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-4G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-4G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6129G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6103G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3096G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20171
  bin: 2.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 7593
  bin: 2.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14919
  bin: 1.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10828
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 1.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2479
  bin: 3.25e1
  variant carriers: 0
hgvs: c.641-4G>A
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

5-150512137-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512137
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512137
    reference: chr 5
allele count: 112
allele frequency: 1.156522996220648e-3
allele num: 96842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-5C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6130C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-5C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-5C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-5C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-5C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6777C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6102C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3097C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 16193
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18716
  bin: 2.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 11186
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2331
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 7.5e0
  variant carriers: 2
hgvs: c.641-5C>T
num of homozygotes: 1
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

5-150512145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512145
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512145
    reference: chr 5
allele count: 8
allele frequency: 8.62775548940943e-5
allele num: 92724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6094C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-13C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6769C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-13C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-13C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-13C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6138C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-13C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3105C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21758
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12442
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1455
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

5-150512147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512147
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512147
    reference: chr 5
allele count: 1
allele frequency: 1.079354114497885e-5
allele num: 92648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3107C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6092C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-15C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6767C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-15C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-15C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-15C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.263-6140C>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-15C>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12553
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21803
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4273
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/5-150512151-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512151
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512151
    reference: chr 5
allele count: 1
allele frequency: 1.094594890431051e-5
allele num: 91358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-19G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-19G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-19G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.262+6144G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-19G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6088G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3111G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6763G>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-19G>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23031
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1760
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4609
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

5-150512154-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512154
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512154
    reference: chr 5
allele count: 1
allele frequency: 1.113660155466958e-5
allele num: 89794
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-22C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-22C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3114C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.262+6141C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6085C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-22C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6760C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-22C>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-22C>G
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

5-150512161-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512161
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512161
    reference: chr 5
allele count: 1
allele frequency: 1.154441135046524e-5
allele num: 86622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-29A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-29A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.262+6134A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6078A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-29A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6753A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-29A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3121A>T
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-29A>T
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6043
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14051
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27354
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/5-150512172-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512172
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512173
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 77556
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6066_318+6067insT
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-41_641-40insT
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.262+6122_262+6123insT
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6741_204+6742insT
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-41_641-40insT
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-41_545-40insT
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3133_225-3132insT
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-41_*70-40insT
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-41_231-40insT
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17208
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5509
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6175
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3435
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

5-150512175-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512175
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512175
    reference: chr 5
allele count: 1
allele frequency: 1.344953733591565e-5
allele num: 74352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6064A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3135A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6739A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-43A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-43A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-43A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.262+6120A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-43A>G
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-43A>G
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20576
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18701
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3565
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3843
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

5-150512179-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512179
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512179
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 71020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-47G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6060G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-47G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-47G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3139G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-47G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.262+6116G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6735G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-47G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19897
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3608
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

5-150512180-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512180
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512180
    reference: chr 5
allele count: 1
allele frequency: 1.422110981541e-5
allele num: 70318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-48G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-48G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-48G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6734G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-48G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3140G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.262+6115G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6059G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-48G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7952
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20085
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17861
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6156
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

5-150512181-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150512181
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 150512181
    reference: chr 5
allele count: 4
allele frequency: 5.751588876427113e-5
allele num: 69546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430826
  ensembl transcript: ENST00000517677
  gene symbol: ANXA6
  hgvsc: ENST00000517677.1:c.*70-49G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000428916
  ensembl transcript: ENST00000517486
  gene symbol: ANXA6
  hgvsc: ENST00000517486.1:c.318+6058G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000366980
  ensembl transcript: ENST00000377751
  gene symbol: ANXA6
  hgvsc: ENST00000377751.5:c.204+6733G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430663
  ensembl transcript: ENST00000519644
  gene symbol: ANXA6
  hgvsc: ENST00000519644.2:c.262+6114G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430517
  ensembl transcript: ENST00000523714
  gene symbol: ANXA6
  hgvsc: ENST00000523714.1:c.545-49G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl transcript: ENST00000517707
  gene symbol: ANXA6
  hgvsc: ENST00000517707.1:n.231-49G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000348889
  ensembl transcript: ENST00000356496
  gene symbol: ANXA6
  hgvsc: ENST00000356496.5:c.641-49G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000346550
  ensembl transcript: ENST00000354546
  gene symbol: ANXA6
  hgvsc: ENST00000354546.5:c.641-49G>A
  variant of: http://identifiers.org/hgnc/544
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197043
  ensembl protein: ENSP00000430420
  ensembl transcript: ENST00000521512
  gene symbol: ANXA6
  hgvsc: ENST00000521512.1:c.225-3141G>A
  variant of: http://identifiers.org/hgnc/544
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20168
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19318
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 3127
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3608
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2572
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 501
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3631
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 283
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2958
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25834
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.150537634408602e-4
allele num: 4650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.97e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

DP
type: SiteQuality
SIO_000300: 7.41222e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

QD
type: SiteQuality
SIO_000300: 1.146e1

VQSLOD
type: SiteQuality
SIO_000300: 2.73e0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 293
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 655
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variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 563
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 16196
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.081e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

FS
type: SiteQuality
SIO_000300: 8.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.816456e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.084e0

VQSLOD
type: SiteQuality
SIO_000300: 4.47e-1

GenotypeQuality
all individuals: 53148
bin: 9.75e1
variant carriers: 131

GenotypeQuality
all individuals: 157
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2059
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.16827041697508e-4
allele num: 16212
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 115
allele frequency: 1.727401087511641e-3
allele num: 66574
num of homozygotes: 0

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

Other
type: Population
allele count: 2
allele frequency: 2.247191011235955e-3
allele num: 890
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

DP
type: SiteQuality
SIO_000300: 4.822303e6

QD
type: SiteQuality
SIO_000300: 1.328e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.83e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.523e0

VQSLOD
type: SiteQuality
SIO_000300: 4.19e0

GenotypeQuality
all individuals: 505
bin: 8.25e1
variant carriers: 9

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

GenotypeQuality
all individuals: 53
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1798
bin: 6.25e1
variant carriers: 9

GenotypeQuality
all individuals: 532
bin: 7.75e1
variant carriers: 12

GenotypeQuality
all individuals: 394
bin: 7.25e1
variant carriers: 7

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 508
bin: 9.25e1
variant carriers: 23

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 8.75e1
variant carriers: 10

GenotypeQuality
all individuals: 193
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 106
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 13

GenotypeQuality
all individuals: 54650
bin: 9.75e1
variant carriers: 15843

European (Non-Finnish)
type: Population
allele count: 8673
allele frequency: 1.301822220887995e-1
allele num: 66622
num of homozygotes: 569

African
type: Population
allele count: 807
allele frequency: 8.234693877551021e-2
allele num: 9800
num of homozygotes: 43

European (Finnish)
type: Population
allele count: 1179
allele frequency: 1.783121597096189e-1
allele num: 6612
num of homozygotes: 121

East Asian
type: Population
allele count: 2172
allele frequency: 2.52499418739828e-1
allele num: 8602
num of homozygotes: 272

Latino
type: Population
allele count: 1557
allele frequency: 1.346187100121044e-1
allele num: 11566
num of homozygotes: 99

Other
type: Population
allele count: 139
allele frequency: 1.554809843400447e-1
allele num: 894
num of homozygotes: 10

South Asian
type: Population
allele count: 2797
allele frequency: 1.715109148883983e-1
allele num: 16308
num of homozygotes: 267

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.078e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.86e-2

DP
type: SiteQuality
SIO_000300: 5.250403e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.56e1

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 150
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variant carriers: 0

GenotypeQuality
all individuals: 106
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variant carriers: 0

GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 139
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GenotypeQuality
all individuals: 797
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variant carriers: 0

GenotypeQuality
all individuals: 539
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variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52773
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 748
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
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: 11572
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
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: 16328
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.275e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 4.539632e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.17e0

FS
type: SiteQuality
SIO_000300: 8.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.177e0

VQSLOD
type: SiteQuality
SIO_000300: 3.48e-1

GenotypeQuality
all individuals: 51
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 751
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 728
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52771
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 574
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 7.75e1
variant carriers: 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: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.997361161089121e-5
allele num: 66696
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.077e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

DP
type: SiteQuality
SIO_000300: 4.547848e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.401e0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3068
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52771
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 807
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
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variant carriers: 0

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

GenotypeQuality
all individuals: 753
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
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: 2
allele frequency: 2.040816326530612e-4
allele num: 9800
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.409999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.02e-1

DP
type: SiteQuality
SIO_000300: 4.54813e6

FS
type: SiteQuality
SIO_000300: 5.449e0

MQRankSum
type: SiteQuality
SIO_000300: -1.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

QD
type: SiteQuality
SIO_000300: 1.171e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.349e0

GenotypeQuality
all individuals: 753
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 420
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 807
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 729
bin: 8.25e1
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GenotypeQuality
all individuals: 1176
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 52771
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3068
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 66704
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.819725827975252e-4
allele num: 16486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 4.54813e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.349e0

QD
type: SiteQuality
SIO_000300: 1.171e1

FS
type: SiteQuality
SIO_000300: 5.449e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.02e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.67e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 9.409999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
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GenotypeQuality
all individuals: 46
bin: 7.5e0
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GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

GenotypeQuality
all individuals: 806
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variant carriers: 0

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

GenotypeQuality
all individuals: 3086
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 0
bin: 1.25e1
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GenotypeQuality
all individuals: 52769
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 420
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variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997961386257345e-5
allele num: 66712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
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: 16490
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.48e-1

DP
type: SiteQuality
SIO_000300: 4.548306e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-1

QD
type: SiteQuality
SIO_000300: 1.219e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.631e0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.995743022454058e-5
allele num: 66714
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: 9800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

DP
type: SiteQuality
SIO_000300: 4.548328e6

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

FS
type: SiteQuality
SIO_000300: 1.144e0

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.222e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52767
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: 8626
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.328e1

FS
type: SiteQuality
SIO_000300: 1.216e0

DP
type: SiteQuality
SIO_000300: 4.548286e6

VQSLOD
type: SiteQuality
SIO_000300: 6.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e0

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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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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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
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: 66722
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.01e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

DP
type: SiteQuality
SIO_000300: 4.548396e6

QD
type: SiteQuality
SIO_000300: 1.405e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

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

GenotypeQuality
all individuals: 577
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52767
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.41e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.203e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.351e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.66e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 4.548521e6

GenotypeQuality
all individuals: 2
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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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: 2

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: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
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: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.548521e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.351e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -6.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.41e-1

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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bin: 3.25e1
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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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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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.898e1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.981e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
type: SiteQuality
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ClippingRankSum
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SIO_000300: 1.24e0

BaseQRankSum
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SIO_000300: -2.688e0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.333e1

FS
type: SiteQuality
SIO_000300: 1.539e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.701e0

VQSLOD
type: SiteQuality
SIO_000300: 7.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 4.548538e6

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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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bin: 3.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.47e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.211e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

GenotypeQuality
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bin: 9.25e1
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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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997152704930316e-5
allele num: 66730
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.221e0

InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
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SIO_000300: 7.31e-1

QD
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SIO_000300: 1.247e1

MQRankSum
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SIO_000300: 1.17e0

DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.041232904674423e-4
allele num: 9798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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QD
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DP
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FS
type: SiteQuality
SIO_000300: 1.101e0

MQRankSum
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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SIO_000300: -2.8e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9798
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.318571759795966e-4
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
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 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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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
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: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.137e0

MQRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.126e0

QD
type: SiteQuality
SIO_000300: 1.331e1

DP
type: SiteQuality
SIO_000300: 4.548217e6

MQ
type: SiteQuality
SIO_000300: 5.986e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-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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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
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QD
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InbreedingCoeff
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BaseQRankSum
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FS
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SIO_000300: 1.943e0

MQRankSum
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ClippingRankSum
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DP
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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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Other
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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 frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056935190793458e-5
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African
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allele count: 2
allele frequency: 2.040816326530612e-4
allele num: 9800
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European (Non-Finnish)
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allele count: 9
allele frequency: 1.348678295270635e-4
allele num: 66732
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 4.637143519591931e-4
allele num: 8626
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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Other
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ClippingRankSum
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FS
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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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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variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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Other
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African
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FS
type: SiteQuality
SIO_000300: 8.32e-1

MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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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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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
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: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

QD
type: SiteQuality
SIO_000300: 1.375e1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 7.414e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.342e0

VQSLOD
type: SiteQuality
SIO_000300: -6.389e-1

DP
type: SiteQuality
SIO_000300: 4.547104e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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: 5.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52766
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 2
allele frequency: 1.213297743266198e-4
allele num: 16484
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: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.902e1

FS
type: SiteQuality
SIO_000300: 1.0658e1

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.277e0

QD
type: SiteQuality
SIO_000300: 1.033e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-2

DP
type: SiteQuality
SIO_000300: 4.546402e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.67e-2

FS
type: SiteQuality
SIO_000300: 1.1908e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.526e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.157e0

VQSLOD
type: SiteQuality
SIO_000300: -1.49e0

QD
type: SiteQuality
SIO_000300: 1.158e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 4.546341e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 570
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52765
bin: 9.75e1
variant carriers: 7

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
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: 4
allele frequency: 4.637143519591931e-4
allele num: 8626
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 1.149e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.546513e6

GenotypeQuality
all individuals: 52765
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
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

East Asian
type: Population
allele count: 2
allele frequency: 2.318571759795966e-4
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.857e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.836e0

QD
type: SiteQuality
SIO_000300: 1.34e1

DP
type: SiteQuality
SIO_000300: 4.546003e6

FS
type: SiteQuality
SIO_000300: 6.820000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.392e0

MQRankSum
type: SiteQuality
SIO_000300: 3.84e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.32e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e0

QD
type: SiteQuality
SIO_000300: 1.427e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e0

FS
type: SiteQuality
SIO_000300: 6.0e0

DP
type: SiteQuality
SIO_000300: 4.544293e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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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: 6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.496027105634013e-5
allele num: 66702
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.55e-1

DP
type: SiteQuality
SIO_000300: 4.543669e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.801e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.36e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-1

DP
type: SiteQuality
SIO_000300: 4.541159e6

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.334e1

MQRankSum
type: SiteQuality
SIO_000300: 9.51e-1

GenotypeQuality
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bin: 5.25e1
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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variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999130252226854e-5
allele num: 66686
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 4.541159e6

MQRankSum
type: SiteQuality
SIO_000300: 9.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.073e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-1

GenotypeQuality
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.541149e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.739e0

FS
type: SiteQuality
SIO_000300: 1.3705e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

QD
type: SiteQuality
SIO_000300: 1.362e1

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

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 3.25e1
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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
all individuals: 260
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variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
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: 6.078288353999514e-5
allele num: 16452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.541464e6

VQSLOD
type: SiteQuality
SIO_000300: 5.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: -1.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

QD
type: SiteQuality
SIO_000300: 1.641e1

FS
type: SiteQuality
SIO_000300: 3.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

GenotypeQuality
all individuals: 5101
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 436
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GenotypeQuality
all individuals: 1392
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3382
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5046
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.780580417683754e-5
allele num: 29496
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.28e-1

FS
type: SiteQuality
SIO_000300: 1.824e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.16e-2

QD
type: SiteQuality
SIO_000300: 1.336e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e0

DP
type: SiteQuality
SIO_000300: 7.13912e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

GenotypeQuality
all individuals: 499
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 283
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.277184243298158e-5
allele num: 30514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3562
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.73e-1

FS
type: SiteQuality
SIO_000300: 1.103e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

DP
type: SiteQuality
SIO_000300: 7.43859e5

QD
type: SiteQuality
SIO_000300: 1.228e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.552e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.567e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

GenotypeQuality
all individuals: 548
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1462
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 585
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variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3910
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.745810055865922e-4
allele num: 5728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4488
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

DP
type: SiteQuality
SIO_000300: 8.59936e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.195e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

MQ
type: SiteQuality
SIO_000300: 5.787e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

GenotypeQuality
all individuals: 625
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1395
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
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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
all individuals: 17831
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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: 510
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1781
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4648
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.928268414963363e-4
allele num: 5186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4156
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6136
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
type: SiteQuality
SIO_000300: 9.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 6.628e0

QD
type: SiteQuality
SIO_000300: 1.125e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.288e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

DP
type: SiteQuality
SIO_000300: 9.32394e5

GenotypeQuality
all individuals: 313
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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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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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1395
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.012350678274954e-4
allele num: 9878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.210775884529207e-5
allele num: 38382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.125e1

MQRankSum
type: SiteQuality
SIO_000300: 9.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.288e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 6.628e0

DP
type: SiteQuality
SIO_000300: 9.32394e5

GenotypeQuality
all individuals: 255
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3497
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GenotypeQuality
all individuals: 1683
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GenotypeQuality
all individuals: 570
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GenotypeQuality
all individuals: 154
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GenotypeQuality
all individuals: 379
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GenotypeQuality
all individuals: 129
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GenotypeQuality
all individuals: 516
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GenotypeQuality
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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: 508
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GenotypeQuality
all individuals: 316
bin: 8.25e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6258
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.969708968521085e-4
allele num: 10102
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.844337882700111e-4
allele num: 5422
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.082465639316951e-4
allele num: 4802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.535625538820427e-5
allele num: 39438
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

FS
type: SiteQuality
SIO_000300: 4.06e0

QD
type: SiteQuality
SIO_000300: 1.412e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.50863e5

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 214
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variant carriers: 0

GenotypeQuality
all individuals: 20192
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 131
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GenotypeQuality
all individuals: 408
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GenotypeQuality
all individuals: 3221
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1392
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4970
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.459661550570641e-5
allele num: 40656
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.04e0

DP
type: SiteQuality
SIO_000300: 9.71569e5

VQSLOD
type: SiteQuality
SIO_000300: -2.233e0

FS
type: SiteQuality
SIO_000300: 2.933e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

GenotypeQuality
all individuals: 1440
bin: 9.75e1
variant carriers: 56

GenotypeQuality
all individuals: 277
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27904
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 1.135073779795687e-3
allele num: 47574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4762
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.40805406927626e-4
allele num: 7102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.62663906142167e-5
allele num: 11592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7182
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.241e1

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

FS
type: SiteQuality
SIO_000300: 1.334e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.25e0

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.96e-1

DP
type: SiteQuality
SIO_000300: 1.092144e6

GenotypeQuality
all individuals: 108
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 645
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variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.071251035625518e-4
allele num: 4828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.185056902523504e-5
allele num: 48504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6136
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.106415e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

FS
type: SiteQuality
SIO_000300: 6.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-1

QD
type: SiteQuality
SIO_000300: 1.116e1

GenotypeQuality
all individuals: 1388
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1318
bin: 2.75e1
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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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
all individuals: 12146
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.830630102881412e-5
allele num: 54626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12730
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

QD
type: SiteQuality
SIO_000300: 1.641e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.946e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.371e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.407e0

DP
type: SiteQuality
SIO_000300: 1.207019e6

GenotypeQuality
all individuals: 721
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 595
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GenotypeQuality
all individuals: 142
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GenotypeQuality
all individuals: 11125
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 37297
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variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55972
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.262307498106539e-4
allele num: 7922
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.134e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

QD
type: SiteQuality
SIO_000300: 4.38e0

VQSLOD
type: SiteQuality
SIO_000300: -2.143e0

DP
type: SiteQuality
SIO_000300: 1.228192e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

FS
type: SiteQuality
SIO_000300: 6.264e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

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

GenotypeQuality
all individuals: 1000
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
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variant carriers: 0

GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 38748
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 164
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GenotypeQuality
all individuals: 750
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GenotypeQuality
all individuals: 3018
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
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GenotypeQuality
all individuals: 650
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8048
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5586
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.05999576001696e-4
allele num: 9434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.693e0

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.252274e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

FS
type: SiteQuality
SIO_000300: 4.964e0

VQSLOD
type: SiteQuality
SIO_000300: -2.221e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

GenotypeQuality
all individuals: 695
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 810
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 367
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variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60862
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5954
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.83671060397403e-5
allele num: 10166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14050
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

DP
type: SiteQuality
SIO_000300: 1.324083e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

FS
type: SiteQuality
SIO_000300: 5.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.068e1

GenotypeQuality
all individuals: 303
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.5e0
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 7209
bin: 2.25e1
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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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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 367
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.64306135191088e-5
allele num: 60862
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 5.893446487505894e-4
allele num: 8484
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.117437722419929e-5
allele num: 14050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5954
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

FS
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 1.324083e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

QD
type: SiteQuality
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GenotypeQuality
all individuals: 727
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 41868
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GenotypeQuality
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GenotypeQuality
all individuals: 711
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GenotypeQuality
all individuals: 3475
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GenotypeQuality
all individuals: 554
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GenotypeQuality
all individuals: 7195
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GenotypeQuality
all individuals: 332
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GenotypeQuality
all individuals: 215
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GenotypeQuality
all individuals: 140
bin: 8.75e1
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GenotypeQuality
all individuals: 304
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61262
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5986
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.798157946306095e-5
allele num: 10206
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.247816321437484e-4
allele num: 8014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.639e0

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.64e-1

DP
type: SiteQuality
SIO_000300: 1.327189e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.69e-1

FS
type: SiteQuality
SIO_000300: 1.2339e1

QD
type: SiteQuality
SIO_000300: 9.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 747
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3204
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variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5954
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.823182711198428e-5
allele num: 10180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61076
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.154e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.118e0

VQSLOD
type: SiteQuality
SIO_000300: -2.624e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.68e-1

DP
type: SiteQuality
SIO_000300: 1.319263e6

QD
type: SiteQuality
SIO_000300: 3.15e0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.683501683501684e-4
allele num: 5940
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14122
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.921259842519685e-5
allele num: 60960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7936
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e-1

QD
type: SiteQuality
SIO_000300: 1.118e1

DP
type: SiteQuality
SIO_000300: 1.316592e6

VQSLOD
type: SiteQuality
SIO_000300: 3.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 39890
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.099247479767145e-5
allele num: 14086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7922
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.686909581646424e-4
allele num: 5928
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.306e0

DP
type: SiteQuality
SIO_000300: 1.311346e6

VQSLOD
type: SiteQuality
SIO_000300: 2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.93e0

GenotypeQuality
all individuals: 12891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 738
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variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5698
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.275902211874272e-5
allele num: 13744
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.242817e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.605e0

QD
type: SiteQuality
SIO_000300: 5.66e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1382
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
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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
all individuals: 200
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GenotypeQuality
all individuals: 586
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5542
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.85e-1

FS
type: SiteQuality
SIO_000300: 2.482e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.828e0

QD
type: SiteQuality
SIO_000300: 4.61e0

DP
type: SiteQuality
SIO_000300: 1.187041e6

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

GenotypeQuality
all individuals: 507
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 380
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GenotypeQuality
all individuals: 2053
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 3.732271709380443e-4
allele num: 8038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.803751803751804e-4
allele num: 5544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.791672527781685e-5
allele num: 56872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-1

DP
type: SiteQuality
SIO_000300: 1.186273e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

FS
type: SiteQuality
SIO_000300: 1.725e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.041e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.276e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

GenotypeQuality
all individuals: 243
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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
all individuals: 537
bin: 7.5e0
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8862
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.5642965204236e-5
allele num: 13220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7120
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

QD
type: SiteQuality
SIO_000300: 8.98e0

VQSLOD
type: SiteQuality
SIO_000300: 6.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

FS
type: SiteQuality
SIO_000300: 9.62e-1

DP
type: SiteQuality
SIO_000300: 1.128592e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e-1

GenotypeQuality
all individuals: 24774
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 531
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GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 375
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GenotypeQuality
all individuals: 302
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GenotypeQuality
all individuals: 200
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GenotypeQuality
all individuals: 229
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 1505
bin: 9.75e1
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GenotypeQuality
all individuals: 354
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variant carriers: 1

GenotypeQuality
all individuals: 551
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GenotypeQuality
all individuals: 131
bin: 8.75e1
variant carriers: 2

East Asian
type: Population
allele count: 132
allele frequency: 1.884637350085665e-2
allele num: 7004
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.646042221168921e-5
allele num: 54854
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13076
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.377410468319559e-3
allele num: 726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7788
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.299908003679853e-4
allele num: 8696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5418
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 2.133e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.108973e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-2

QD
type: SiteQuality
SIO_000300: 1.168e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 106

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

East Asian
type: Population
allele count: 41
allele frequency: 5.947200464171743e-3
allele num: 6894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 68
allele frequency: 5.228356143318468e-3
allele num: 13006
num of homozygotes: 1

Other
type: Population
allele count: 2
allele frequency: 2.754820936639119e-3
allele num: 726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.835535976505139e-5
allele num: 54480
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.211e1

VQSLOD
type: SiteQuality
SIO_000300: 4.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.54e0

FS
type: SiteQuality
SIO_000300: 6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

DP
type: SiteQuality
SIO_000300: 1.086822e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.533565924165165e-4
allele num: 52166
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7504
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.201e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

DP
type: SiteQuality
SIO_000300: 9.83235e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.531e0

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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.919680565153959e-5
allele num: 52092
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5216
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

DP
type: SiteQuality
SIO_000300: 9.81564e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.775e0

FS
type: SiteQuality
SIO_000300: 2.741e0

VQSLOD
type: SiteQuality
SIO_000300: -3.01e-2

QD
type: SiteQuality
SIO_000300: 8.130000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.83e0

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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variant carriers: 0

GenotypeQuality
all individuals: 292
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GenotypeQuality
all individuals: 198
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7444
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.064516129032258e-5
allele num: 12400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5142
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.977e0

DP
type: SiteQuality
SIO_000300: 9.54583e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.309e0

VQSLOD
type: SiteQuality
SIO_000300: -1.367e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.31e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 482
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GenotypeQuality
all individuals: 374
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.978865714172636e-5
allele num: 50534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5070
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.648e0

VQSLOD
type: SiteQuality
SIO_000300: -3.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

DP
type: SiteQuality
SIO_000300: 9.23237e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.225e0

QD
type: SiteQuality
SIO_000300: 4.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.72e-1

GenotypeQuality
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bin: 5.25e1
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
all individuals: 477
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.049684348610314e-5
allele num: 48788
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5994
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4938
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11850
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

MQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.458e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

DP
type: SiteQuality
SIO_000300: 8.77874e5

QD
type: SiteQuality
SIO_000300: 7.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

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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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10990
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5992
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43790
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.754e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.55e0

VQSLOD
type: SiteQuality
SIO_000300: -4.536e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

DP
type: SiteQuality
SIO_000300: 8.14713e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.383108526762309e-5
allele num: 41962
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5624
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

DP
type: SiteQuality
SIO_000300: 8.03301e5

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 8.1e-3

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.47e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 126
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GenotypeQuality
all individuals: 2779
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1371
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40018
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5198
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 7.95238e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.59e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 1.298e1

GenotypeQuality
all individuals: 4463
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3611
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1371
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5302
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6278
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39634
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.668335001668335e-4
allele num: 5994
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.52e-2

DP
type: SiteQuality
SIO_000300: 7.94251e5

FS
type: SiteQuality
SIO_000300: 3.237e0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.461e0

QD
type: SiteQuality
SIO_000300: 1.38e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.02e-1