15-60644723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60644723
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60644723
    reference: chr 15
allele count: 8
allele frequency: 8.353346559465386e-5
allele num: 95770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.394-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.238-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.238-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.643-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.495-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.589-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.589-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*443-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.589-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.589-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2927-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.589-48G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.589-48G>A
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8686
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13601
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

15-60644724-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60644724
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60644724
    reference: chr 15
allele count: 6
allele frequency: 6.343970056461333e-5
allele num: 94578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.394-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.643-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.495-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.589-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*443-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.589-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2927-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.589-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.589-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.238-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.589-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.589-49C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.238-49C>T
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13511
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8686
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-60644726-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60644726
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60644727
    reference: chr 15
allele count: 10
allele frequency: 1.276943508019205e-4
allele num: 78312
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.589-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.238-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*443-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2927-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.238-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.589-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.589-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.643-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.589-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.589-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.495-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.394-52dupT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.589-52dupT
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20024
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13365
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11191
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7801
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

15-60644726-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60644726
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60644726
    reference: chr 15
allele count: 3
allele frequency: 3.830830524057616e-5
allele num: 78312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.238-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.589-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.589-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*443-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.238-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.589-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2927-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.394-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.589-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.589-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.495-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.589-51G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.643-51G>C
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13365
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7801
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-60644726-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60644726
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60644725
    reference: chr 15
allele count: 138
allele frequency: 1.762182041066503e-3
allele num: 78312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.394-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.238-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.589-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.643-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.589-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.238-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.589-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.495-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*443-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2927-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.589-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.589-52delT
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.589-52delT
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20024
  bin: 1.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13365
  bin: 1.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 7801
  bin: 2.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 11191
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: CA
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

15-60646305-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646305
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646305
    reference: chr 15
allele count: 3
allele frequency: 2.59000259000259e-5
allele num: 115830
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2926+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.588+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.237+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.494+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.588+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.588+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.588+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.393+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.588+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.642+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.588+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*442+48C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.237+48C>G
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12233
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8211
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

15-60646313-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646313
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646313
    reference: chr 15
allele count: 2
allele frequency: 1.718744628923035e-5
allele num: 116364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.393+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.588+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.588+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.642+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.237+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2926+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.588+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.588+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*442+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.588+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.588+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.494+40G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.237+40G>C
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6527
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

15-60646316-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646316
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646316
    reference: chr 15
allele count: 59
allele frequency: 5.040408700258001e-4
allele num: 117054
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.642+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.588+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.393+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.588+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.588+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.588+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.237+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*442+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.588+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.237+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.494+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2926+37C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.588+37C>T
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14128
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 24542
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 1.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/15-60646320-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646320
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646320
    reference: chr 15
allele count: 2
allele frequency: 1.705233361185478e-5
allele num: 117286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.588+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*442+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.588+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.588+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.588+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.393+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.588+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.494+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2926+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.642+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.588+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.237+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.237+33T>G
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

15-60646331-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646331
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646331
    reference: chr 15
allele count: 1
allele frequency: 8.444376889429329e-6
allele num: 118422
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*442+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.642+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2926+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.588+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.588+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.588+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.237+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.588+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.393+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.237+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.588+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.494+22T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.588+22T>C
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

15-60646354-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646354
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646354
    reference: chr 15
allele count: 2
allele frequency: 1.661654010401954e-5
allele num: 120362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.587G>A
  hgvsp: ENSP00000379342.3:p.Arg196Gln
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.236G>A
  hgvsp: ENSP00000453039.1:p.Arg79Gln
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.392G>A
  hgvsp: ENSP00000454096.1:p.Arg131Gln
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2925G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.641G>A
  hgvsp: ENSP00000346032.3:p.Arg214Gln
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*441G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*198G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.236G>A
  hgvsp: ENSP00000453841.1:p.Arg79Gln
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.587G>A
  hgvsp: ENSP00000387545.2:p.Arg196Gln
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.587G>A
  hgvsp: ENSP00000453754.1:p.Arg196Gln
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.236G>A
  hgvsp: ENSP00000453925.1:p.Arg79Gln
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.587G>A
  hgvsp: ENSP00000453859.1:p.Arg196Gln
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.587G>A
  hgvsp: ENSP00000453556.1:p.Arg196Gln
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.587G>A
  hgvsp: ENSP00000411352.2:p.Arg196Gln
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.493G>A
  hgvsp: ENSP00000453464.1:p.Arg165Gln
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg214Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

15-60646355-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646355
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646355
    reference: chr 15
allele count: 1
allele frequency: 8.304820117596252e-6
allele num: 120412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.586C>T
  hgvsp: ENSP00000453556.1:p.Arg196Trp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.586C>T
  hgvsp: ENSP00000379342.3:p.Arg196Trp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2924C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.235C>T
  hgvsp: ENSP00000453039.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*440C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.586C>T
  hgvsp: ENSP00000387545.2:p.Arg196Trp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.640C>T
  hgvsp: ENSP00000346032.3:p.Arg214Trp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.586C>T
  hgvsp: ENSP00000453754.1:p.Arg196Trp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.492C>T
  hgvsp: ENSP00000453464.1:p.Arg165Trp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.586C>T
  hgvsp: ENSP00000453859.1:p.Arg196Trp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.391C>T
  hgvsp: ENSP00000454096.1:p.Arg131Trp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.235C>T
  hgvsp: ENSP00000453925.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*197C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.586C>T
  hgvsp: ENSP00000411352.2:p.Arg196Trp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.235C>T
  hgvsp: ENSP00000453841.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg214Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-60646377-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646377
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646377
    reference: chr 15
allele count: 2
allele frequency: 1.657495193263939e-5
allele num: 120664
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.564T>C
  hgvsp: ENST00000559818.1:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.213T>C
  hgvsp: ENST00000558998.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.564T>C
  hgvsp: ENST00000560367.2:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.564T>C
  hgvsp: ENST00000396024.3:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*418T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.564T>C
  hgvsp: ENST00000421017.2:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.213T>C
  hgvsp: ENST00000558985.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.369T>C
  hgvsp: ENST00000558132.1:c.369T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.470T>C
  hgvsp: ENST00000559176.1:c.470T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.213T>C
  hgvsp: ENST00000560466.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.564T>C
  hgvsp: ENST00000560014.1:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.564T>C
  hgvsp: ENST00000451270.2:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*175T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.618T>C
  hgvsp: ENST00000332680.4:c.618T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2902T>C
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr206Tyr
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-60646381-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646381
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646381
    reference: chr 15
allele count: 16
allele frequency: 1.326084073730274e-4
allele num: 120656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*171A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.209A>G
  hgvsp: ENSP00000453841.1:p.Asp70Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.560A>G
  hgvsp: ENSP00000379342.3:p.Asp187Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.209A>G
  hgvsp: ENSP00000453925.1:p.Asp70Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.560A>G
  hgvsp: ENSP00000387545.2:p.Asp187Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.466A>G
  hgvsp: ENSP00000453464.1:p.Asp156Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.560A>G
  hgvsp: ENSP00000411352.2:p.Asp187Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.365A>G
  hgvsp: ENSP00000454096.1:p.Asp122Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.614A>G
  hgvsp: ENSP00000346032.3:p.Asp205Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.560A>G
  hgvsp: ENSP00000453556.1:p.Asp187Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.560A>G
  hgvsp: ENSP00000453754.1:p.Asp187Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*414A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2898A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.209A>G
  hgvsp: ENSP00000453039.1:p.Asp70Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.560A>G
  hgvsp: ENSP00000453859.1:p.Asp187Gly
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33407
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp205Gly
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS

15-60646382-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646382
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646382
    reference: chr 15
allele count: 1
allele frequency: 8.288712431410904e-6
allele num: 120646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*170G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.364G>A
  hgvsp: ENSP00000454096.1:p.Asp122Asn
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.208G>A
  hgvsp: ENSP00000453925.1:p.Asp70Asn
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.208G>A
  hgvsp: ENSP00000453841.1:p.Asp70Asn
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.465G>A
  hgvsp: ENSP00000453464.1:p.Asp156Asn
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.208G>A
  hgvsp: ENSP00000453039.1:p.Asp70Asn
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.559G>A
  hgvsp: ENSP00000453556.1:p.Asp187Asn
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*413G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.559G>A
  hgvsp: ENSP00000411352.2:p.Asp187Asn
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.559G>A
  hgvsp: ENSP00000379342.3:p.Asp187Asn
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.559G>A
  hgvsp: ENSP00000453754.1:p.Asp187Asn
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2897G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.559G>A
  hgvsp: ENSP00000387545.2:p.Asp187Asn
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.559G>A
  hgvsp: ENSP00000453859.1:p.Asp187Asn
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.613G>A
  hgvsp: ENSP00000346032.3:p.Asp205Asn
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp205Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

15-60646392-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646392
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646392
    reference: chr 15
allele count: 5
allele frequency: 4.150410890678177e-5
allele num: 120470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.549C>T
  hgvsp: ENST00000560367.2:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.603C>T
  hgvsp: ENST00000332680.4:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.354C>T
  hgvsp: ENST00000558132.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.198C>T
  hgvsp: ENST00000558998.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.549C>T
  hgvsp: ENST00000421017.2:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.549C>T
  hgvsp: ENST00000451270.2:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.455C>T
  hgvsp: ENST00000559176.1:c.455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.549C>T
  hgvsp: ENST00000559818.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.198C>T
  hgvsp: ENST00000560466.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.198C>T
  hgvsp: ENST00000558985.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.549C>T
  hgvsp: ENST00000560014.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*160C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.549C>T
  hgvsp: ENST00000396024.3:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*403C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2887C>T
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly201Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

15-60646396-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646396
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646396
    reference: chr 15
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*156A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.545A>G
  hgvsp: ENSP00000411352.2:p.Asp182Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.545A>G
  hgvsp: ENSP00000453859.1:p.Asp182Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.194A>G
  hgvsp: ENSP00000453925.1:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.194A>G
  hgvsp: ENSP00000453039.1:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*399A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.545A>G
  hgvsp: ENSP00000379342.3:p.Asp182Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.545A>G
  hgvsp: ENSP00000453556.1:p.Asp182Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.545A>G
  hgvsp: ENSP00000453754.1:p.Asp182Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.545A>G
  hgvsp: ENSP00000387545.2:p.Asp182Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.599A>G
  hgvsp: ENSP00000346032.3:p.Asp200Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.350A>G
  hgvsp: ENSP00000454096.1:p.Asp117Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.194A>G
  hgvsp: ENSP00000453841.1:p.Asp65Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.451A>G
  hgvsp: ENSP00000453464.1:p.Asp151Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2883A>G
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17853
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp200Gly
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

15-60646404-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646404
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646404
    reference: chr 15
allele count: 1
allele frequency: 8.330001332800213e-6
allele num: 120048
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.591A>T
  hgvsp: ENSP00000346032.3:p.Arg197Ser
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.186A>T
  hgvsp: ENSP00000453841.1:p.Arg62Ser
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*391A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.537A>T
  hgvsp: ENSP00000453556.1:p.Arg179Ser
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2875A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.443A>T
  hgvsp: ENSP00000453464.1:p.Arg148Ser
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.537A>T
  hgvsp: ENSP00000453859.1:p.Arg179Ser
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.537A>T
  hgvsp: ENSP00000387545.2:p.Arg179Ser
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.537A>T
  hgvsp: ENSP00000379342.3:p.Arg179Ser
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.342A>T
  hgvsp: ENSP00000454096.1:p.Arg114Ser
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*148A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.537A>T
  hgvsp: ENSP00000453754.1:p.Arg179Ser
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.537A>T
  hgvsp: ENSP00000411352.2:p.Arg179Ser
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.186A>T
  hgvsp: ENSP00000453039.1:p.Arg62Ser
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.186A>T
  hgvsp: ENSP00000453925.1:p.Arg62Ser
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg197Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

15-60646409-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646409
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646409
    reference: chr 15
allele count: 157
allele frequency: 1.310911459203099e-3
allele num: 119764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.337A>G
  hgvsp: ENSP00000454096.1:p.Arg113Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.532A>G
  hgvsp: ENSP00000387545.2:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2870A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.181A>G
  hgvsp: ENSP00000453925.1:p.Arg61Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.181A>G
  hgvsp: ENSP00000453841.1:p.Arg61Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.532A>G
  hgvsp: ENSP00000453754.1:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.438A>G
  hgvsp: ENSP00000453464.1:p.Arg147Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.181A>G
  hgvsp: ENSP00000453039.1:p.Arg61Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.532A>G
  hgvsp: ENSP00000453556.1:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.586A>G
  hgvsp: ENSP00000346032.3:p.Arg196Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*143A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.532A>G
  hgvsp: ENSP00000411352.2:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.532A>G
  hgvsp: ENSP00000379342.3:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.532A>G
  hgvsp: ENSP00000453859.1:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*386A>G
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31450
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
hgvs: p.Arg196Gly
num of homozygotes: 5
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

15-60646411-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646411
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646411
    reference: chr 15
allele count: 1
allele frequency: 8.362882183715796e-6
allele num: 119576
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*384G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.530G>A
  hgvsp: ENSP00000453556.1:p.Gly177Asp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.530G>A
  hgvsp: ENSP00000411352.2:p.Gly177Asp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.179G>A
  hgvsp: ENSP00000453925.1:p.Gly60Asp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.436G>A
  hgvsp: ENSP00000453464.1:p.Gly146Asp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.584G>A
  hgvsp: ENSP00000346032.3:p.Gly195Asp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.530G>A
  hgvsp: ENSP00000453754.1:p.Gly177Asp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.530G>A
  hgvsp: ENSP00000453859.1:p.Gly177Asp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.530G>A
  hgvsp: ENSP00000387545.2:p.Gly177Asp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.335G>A
  hgvsp: ENSP00000454096.1:p.Gly112Asp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.530G>A
  hgvsp: ENSP00000379342.3:p.Gly177Asp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2868G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.179G>A
  hgvsp: ENSP00000453039.1:p.Gly60Asp
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*141G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.179G>A
  hgvsp: ENSP00000453841.1:p.Gly60Asp
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly195Asp
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ

15-60646416-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646416
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646416
    reference: chr 15
allele count: 22
allele frequency: 1.847838868450671e-4
allele num: 119058
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-4A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-4A>G
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17750
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.583-4A>G
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ

15-60646416-TGG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646416
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646414
    reference: chr 15
allele count: 1
allele frequency: 8.399267583866688e-6
allele num: 119058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-6_529-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-6_178-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-6_178-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-6_435-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-6_*383-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-6_529-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-6_529-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-6_583-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-6_178-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-6_*140-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-6_529-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-6_334-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-6_529-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-6_529-5delCC
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-6_2867-5delCC
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.583-6_583-5delCC
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: TGG
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

15-60646423-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646423
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646423
    reference: chr 15
allele count: 1
allele frequency: 8.463530646444471e-6
allele num: 118154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-11T>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-11T>A
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4717
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/15-60646428-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646428
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646428
    reference: chr 15
allele count: 1
allele frequency: 8.520790729379687e-6
allele num: 117360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-16T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-16T>G
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

15-60646434-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646434
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646434
    reference: chr 15
allele count: 1
allele frequency: 8.548762139242238e-6
allele num: 116976
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-22G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-22G>A
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8599
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/15-60646439-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646439
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646439
    reference: chr 15
allele count: 2
allele frequency: 1.716856093122274e-5
allele num: 116492
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-27T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-27T>G
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14719
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD

15-60646439-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646439
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646439
    reference: chr 15
allele count: 3
allele frequency: 2.575284139683412e-5
allele num: 116492
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-27T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-27T>C
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19764
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

15-60646441-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646441
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646441
    reference: chr 15
allele count: 1
allele frequency: 8.606296366421674e-6
allele num: 116194
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-29A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-29A>G
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6809
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

15-60646443-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646443
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646443
    reference: chr 15
allele count: 2
allele frequency: 1.724108205030948e-5
allele num: 116002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-31G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-31G>A
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13613
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

15-60646444-ATTTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646444
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646440
    reference: chr 15
allele count: 2
allele frequency: 1.724108205030948e-5
allele num: 116002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-36_529-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-36_178-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-36_529-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-36_*140-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-36_529-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-36_*383-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-36_2867-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-36_178-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-36_529-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-36_529-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-36_178-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-36_583-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-36_334-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-36_529-33delGAAA
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-36_435-33delGAAA
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13257
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: ATTTC
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

15-60646447-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646447
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646447
    reference: chr 15
allele count: 2
allele frequency: 1.731811648165145e-5
allele num: 115486
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-35A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-35A>C
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/15-60646448-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646448
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646448
    reference: chr 15
allele count: 2
allele frequency: 1.734816022760786e-5
allele num: 115286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-36G>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-36G>T
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

15-60646449-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646449
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646449
    reference: chr 15
allele count: 1
allele frequency: 8.706554294072578e-6
allele num: 114856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-37A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-37A>G
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

15-60646455-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646455
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646455
    reference: chr 15
allele count: 1
allele frequency: 8.770698849284312e-6
allele num: 114016
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-43A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-43A>G
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16399
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-60646462-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60646462
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60646462
    reference: chr 15
allele count: 1
allele frequency: 8.877210425395924e-6
allele num: 112648
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*383-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.334-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.583-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.529-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.178-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.178-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.529-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*140-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2867-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.529-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.529-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.529-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.435-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.178-50T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.529-50T>G
  variant of: http://identifiers.org/hgnc/537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

15-60647958-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60647958
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60647958
    reference: chr 15
allele count: 1
allele frequency: 4.930966469428008e-5
allele num: 20280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.745A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+160A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+160A>G
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22642
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

15-60647959-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60647959
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60647959
    reference: chr 15
allele count: 1
allele frequency: 4.91497100167109e-5
allele num: 20346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.744A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+159A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+159A>G
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25129
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-60647965-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60647965
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60647965
    reference: chr 15
allele count: 1
allele frequency: 4.630915995183848e-5
allele num: 21594
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.738G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+153G>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+153G>C
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20574
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

15-60647969-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60647969
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60647969
    reference: chr 15
allele count: 2
allele frequency: 8.703220191470844e-5
allele num: 22980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.734C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+149C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+149C>T
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17439
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

15-60647971-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60647971
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60647971
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 24252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.732T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+147T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+147T>C
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15595
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

15-60647978-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60647978
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60647978
    reference: chr 15
allele count: 1
allele frequency: 3.582688449412439e-5
allele num: 27912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.725C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+140C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+140C>T
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS

15-60647985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60647985
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60647985
    reference: chr 15
allele count: 5
allele frequency: 1.513500423780119e-4
allele num: 33036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.718G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+133G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+133G>A
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

15-60647996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60647996
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60647996
    reference: chr 15
allele count: 2
allele frequency: 4.482897745102434e-5
allele num: 44614
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.707T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+122T>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+122T>C
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

15-60648004-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648004
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648004
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 54720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.699G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+114G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+114G>A
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 17410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30673
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP

15-60648006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648006
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648006
    reference: chr 15
allele count: 4
allele frequency: 6.786332326694038e-5
allele num: 58942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.697C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+112C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+112C>T
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19363
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

15-60648020-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648020
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648020
    reference: chr 15
allele count: 1
allele frequency: 1.196888090963495e-5
allele num: 83550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.683C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+98C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+98C>T
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ

15-60648022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648022
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648022
    reference: chr 15
allele count: 1
allele frequency: 1.15233924867481e-5
allele num: 86780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.681G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+96G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+96G>A
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31740
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/15-60648023-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648023
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648023
    reference: chr 15
allele count: 1
allele frequency: 1.119946242580356e-5
allele num: 89290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.680T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+95T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+95T>G
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

15-60648024-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648024
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648024
    reference: chr 15
allele count: 1
allele frequency: 1.096587419949118e-5
allele num: 91192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.679G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+94G>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+94G>A
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

15-60648027-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648027
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648027
    reference: chr 15
allele count: 1
allele frequency: 1.034853878632337e-5
allele num: 96632
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.676C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+91C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+91C>G
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-60648028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648028
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648028
    reference: chr 15
allele count: 3
allele frequency: 3.055238715985009e-5
allele num: 98192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.675C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+90C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+90C>T
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36718
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

15-60648041-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648041
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648041
    reference: chr 15
allele count: 2
allele frequency: 1.780056249777493e-5
allele num: 112356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.662A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+77A>C
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+77A>C
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43126
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

15-60648050-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648050
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648050
    reference: chr 15
allele count: 5
allele frequency: 4.227328835455452e-5
allele num: 118278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.653C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+68C>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+68C>G
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

15-60648063-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648063
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648063
    reference: chr 15
allele count: 1
allele frequency: 8.280064915708939e-6
allele num: 120772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.640A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+55A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+55A>G
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

15-60648065-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648065
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648065
    reference: chr 15
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.638A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+53A>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+53A>T
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

15-60648065-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648065
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648065
    reference: chr 15
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.638A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+53A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+53A>G
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

15-60648073-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648073
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648073
    reference: chr 15
allele count: 2
allele frequency: 1.649321304283287e-5
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.630C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+45C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+45C>T
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

15-60648076-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648076
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648076
    reference: chr 15
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.627A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+42A>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+42A>G
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

15-60648080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648080
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648080
    reference: chr 15
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.623C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+38C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+38C>T
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-60648085-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648085
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648085
    reference: chr 15
allele count: 5
allele frequency: 4.120313143798929e-5
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.618T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+33T>G
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+33T>G
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

15-60648086-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648086
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648086
    reference: chr 15
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.617C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+32C>A
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+32C>A
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45787
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

15-60648090-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648090
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648090
    reference: chr 15
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.613C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+28C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+28C>T
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9671
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

15-60648092-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648092
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648092
    reference: chr 15
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.611C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+26C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+26C>T
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS

15-60648109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 60648109
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 60648109
    reference: chr 15
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000411352
  ensembl transcript: ENST00000421017
  gene symbol: ANXA2
  hgvsc: ENST00000421017.2:c.528+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453754
  ensembl transcript: ENST00000560014
  gene symbol: ANXA2
  hgvsc: ENST00000560014.1:c.528+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000504475
  gene symbol: ANXA2
  hgvsc: ENST00000504475.2:n.2866+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182718
  ensembl transcript: ENST00000559559
  gene symbol: ANXA2
  hgvsc: ENST00000559559.1:n.594C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453841
  ensembl transcript: ENST00000560466
  gene symbol: ANXA2
  hgvsc: ENST00000560466.1:c.177+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453859
  ensembl transcript: ENST00000559818
  gene symbol: ANXA2
  hgvsc: ENST00000559818.1:c.528+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453925
  ensembl transcript: ENST00000558998
  gene symbol: ANXA2
  hgvsc: ENST00000558998.1:c.177+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000379342
  ensembl transcript: ENST00000396024
  gene symbol: ANXA2
  hgvsc: ENST00000396024.3:c.528+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000346032
  ensembl transcript: ENST00000332680
  gene symbol: ANXA2
  hgvsc: ENST00000332680.4:c.582+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453556
  ensembl transcript: ENST00000560367
  gene symbol: ANXA2
  hgvsc: ENST00000560367.2:c.528+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000452876
  ensembl transcript: ENST00000561022
  gene symbol: ANXA2
  hgvsc: ENST00000561022.1:c.*382+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453464
  ensembl transcript: ENST00000559176
  gene symbol: ANXA2
  hgvsc: ENST00000559176.1:c.434+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000454096
  ensembl transcript: ENST00000558132
  gene symbol: ANXA2
  hgvsc: ENST00000558132.1:c.333+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453039
  ensembl transcript: ENST00000558985
  gene symbol: ANXA2
  hgvsc: ENST00000558985.1:c.177+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000387545
  ensembl transcript: ENST00000451270
  gene symbol: ANXA2
  hgvsc: ENST00000451270.2:c.528+9C>T
  variant of: http://identifiers.org/hgnc/537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182718
  ensembl protein: ENSP00000453356
  ensembl transcript: ENST00000558503
  gene symbol: ANXA2
  hgvsc: ENST00000558503.1:c.*139+9C>T
  variant of: http://identifiers.org/hgnc/537
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

GenotypeDepth
all individuals: 35
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2224
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6175
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14667
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8965
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3788
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6136
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2303
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 176
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2811
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 5445
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.709803014532978e-5
allele num: 51882
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.277904328018223e-4
allele num: 8780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.17813383600377e-4
allele num: 8488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6646
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.266385699752942e-5
allele num: 13762
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

QD
type: SiteQuality
SIO_000300: 1.447e1

FS
type: SiteQuality
SIO_000300: 1.457e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.6e-2

MQ
type: SiteQuality
SIO_000300: 5.635e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 9.70863e5

GenotypeDepth
all individuals: 35
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1154
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 20200
bin: 1.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 206
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2215
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13996
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2875
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4380
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8962
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1342
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 6153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2324
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5074
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.173249902229175e-4
allele num: 51140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5408
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13716
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

FS
type: SiteQuality
SIO_000300: 2.45e0

DP
type: SiteQuality
SIO_000300: 9.68614e5

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
SIO_000300: 5.711e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.163e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

QD
type: SiteQuality
SIO_000300: 1.206e1

VQSLOD
type: SiteQuality
SIO_000300: -2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.84e-1

GenotypeDepth
all individuals: 554
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10791
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 383
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2997
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1765
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6777
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5187
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3278
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5242
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 5329
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2133
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7493
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2794
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2784
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 7.749535027898327e-4
allele num: 6452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.719875395289564e-5
allele num: 42374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4782
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7556
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.698812522490104e-4
allele num: 11116
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

QD
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-2

DP
type: SiteQuality
SIO_000300: 9.72466e5

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.682e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeDepth
all individuals: 387
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2794
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3278
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7493
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2784
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5329
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5187
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1765
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2997
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10791
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6777
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5242
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 9.75e1
variant carriers: 3

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 5.528934758569849e-4
allele num: 5426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4782
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 9.72466e5

MQ
type: SiteQuality
SIO_000300: 5.682e1

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2997
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 501
bin: 5.75e1
variant carriers: 21

GenotypeQuality
all individuals: 5187
bin: 2.75e1
variant carriers: 13

GenotypeQuality
all individuals: 2794
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 414
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 103
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 257
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2784
bin: 4.75e1
variant carriers: 10

GenotypeQuality
all individuals: 3278
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2133
bin: 4.25e1
variant carriers: 15

GenotypeQuality
all individuals: 6777
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10791
bin: 2.25e1
variant carriers: 17

GenotypeQuality
all individuals: 1003
bin: 6.75e1
variant carriers: 9

GenotypeQuality
all individuals: 5329
bin: 1.75e1
variant carriers: 12

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 7.25e1
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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: 14

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4782
num of homozygotes: 0

African
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allele count: 9
allele frequency: 1.191106405505559e-3
allele num: 7556
num of homozygotes: 0

East Asian
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allele count: 6
allele frequency: 1.10578695171397e-3
allele num: 5426
num of homozygotes: 0

Latino
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allele frequency: 1.859888406695598e-3
allele num: 6452
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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South Asian
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allele count: 60
allele frequency: 5.397625044980208e-3
allele num: 11116
num of homozygotes: 0

European (Non-Finnish)
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allele count: 51
allele frequency: 1.203568225798839e-3
allele num: 42374
num of homozygotes: 0

MQ
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DP
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FS
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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SIO_000300: 5.05e-1

QD
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SIO_000300: 1.01e0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.016287954956767e-4
allele num: 9946
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11194
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63564
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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VQSLOD
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.129792494757598e-5
allele num: 63902
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -2.41e-1

ReadPosRankSum
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DP
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MQRankSum
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FS
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MQ
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SIO_000300: 6.0e1

QD
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InbreedingCoeff
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SIO_000300: 3.0e-4

BaseQRankSum
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SIO_000300: -1.5e-1

VQSLOD
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SIO_000300: 3.63e0

GenotypeDepth
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variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 9.984025559105431e-5
allele num: 10016
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.529051987767584e-4
allele num: 6540
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.650644990280969e-4
allele num: 11318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15756
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European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 8.401792382374906e-4
allele num: 64272
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

MQ
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VQSLOD
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InbreedingCoeff
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SIO_000300: 4.5e-3

BaseQRankSum
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SIO_000300: -2.699e0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.46057e6

QD
type: SiteQuality
SIO_000300: 1.409e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15760
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.103469679101236e-5
allele num: 64444
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8296
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Latino
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: 1.78e0

QD
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BaseQRankSum
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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SIO_000300: -5.02e-1

MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11394
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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South Asian
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ClippingRankSum
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DP
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.021513173797438e-5
allele num: 66192
num of homozygotes: 0

East Asian
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African
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Latino
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South Asian
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European (Finnish)
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Other
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InbreedingCoeff
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MQRankSum
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FS
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: -1.19e0

VQSLOD
type: SiteQuality
SIO_000300: -1.529e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 491
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66212
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.697439875872769e-5
allele num: 10312
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.479e0

DP
type: SiteQuality
SIO_000300: 1.584308e6

MQRankSum
type: SiteQuality
SIO_000300: -5.94e-1

FS
type: SiteQuality
SIO_000300: 7.903e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQ
type: SiteQuality
SIO_000300: 5.753e1

QD
type: SiteQuality
SIO_000300: 8.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-1

BaseQRankSum
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SIO_000300: -1.174e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-1

GenotypeDepth
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bin: 2.5e0
variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014681498899641e-5
allele num: 66342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16338
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: 10334
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.304e1

FS
type: SiteQuality
SIO_000300: 8.36e-1

DP
type: SiteQuality
SIO_000300: 1.590398e6

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 16

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

South Asian
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allele count: 16
allele frequency: 9.795518550263255e-4
allele num: 16334
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: 0
allele frequency: 0.0e0
allele num: 66340
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 9.57e-1

DP
type: SiteQuality
SIO_000300: 1.590756e6

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

QD
type: SiteQuality
SIO_000300: 1.033e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

FS
type: SiteQuality
SIO_000300: 2.45e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507477086348288e-5
allele num: 66336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -3.7e-1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.328e0

DP
type: SiteQuality
SIO_000300: 1.590745e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.548537093511277e-5
allele num: 66238
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16306
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.417e0

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -3.0e-4

ReadPosRankSum
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.253e1

DP
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 488
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16292
num of homozygotes: 0

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

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

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

Latino
type: Population
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allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510300247689241e-5
allele num: 66212
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.099e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

FS
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SIO_000300: 1.129e0

BaseQRankSum
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SIO_000300: -8.52e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.33e-1

ReadPosRankSum
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SIO_000300: -1.434e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.586835e6

GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66028
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.161429451632779e-5
allele num: 16230
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DP
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MQ
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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SIO_000300: -7.6e-1

FS
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
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SIO_000300: 1.35e0

QD
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SIO_000300: 8.68e0

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 22

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
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allele count: 96
allele frequency: 8.385744234800839e-3
allele num: 11448
num of homozygotes: 4

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

Other
type: Population
allele count: 5
allele frequency: 5.543237250554324e-3
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
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allele count: 55
allele frequency: 8.351047676890374e-4
allele num: 65860
num of homozygotes: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.183527083848628e-5
allele num: 16172
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

DP
type: SiteQuality
SIO_000300: 1.577634e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
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SIO_000300: 2.34e-1

ReadPosRankSum
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SIO_000300: 3.14e-1

FS
type: SiteQuality
SIO_000300: 1.203e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.97e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 1.317e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521097624045511e-5
allele num: 65742
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -4.722e0

MQRankSum
type: SiteQuality
SIO_000300: -8.62e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.570529e6

MQ
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16056
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

European (Finnish)
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allele count: 3
allele frequency: 4.574565416285453e-4
allele num: 6558
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 19
allele frequency: 2.901737988331959e-4
allele num: 65478
num of homozygotes: 0

ReadPosRankSum
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MQRankSum
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QD
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8544
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European (Non-Finnish)
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allele frequency: 1.527230520174715e-5
allele num: 65478
num of homozygotes: 0

African
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Other
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.538082933431771e-5
allele num: 65016
num of homozygotes: 0

InbreedingCoeff
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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Latino
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Other
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FS
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ClippingRankSum
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ReadPosRankSum
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DP
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MQRankSum
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 64364
num of homozygotes: 0

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

Latino
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African
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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InbreedingCoeff
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BaseQRankSum
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QD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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FS
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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South Asian
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BaseQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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African
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East Asian
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South Asian
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ClippingRankSum
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DP
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QD
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MQ
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FS
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VQSLOD
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GenotypeQuality
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European (Finnish)
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Latino
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African
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East Asian
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Other
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European (Non-Finnish)
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allele frequency: 1.566710534561634e-5
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MQRankSum
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

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

East Asian
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allele num: 8212
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Latino
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European (Non-Finnish)
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European (Finnish)
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ReadPosRankSum
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 63452
num of homozygotes: 0

East Asian
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South Asian
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allele num: 15410
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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ReadPosRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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Other
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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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FS
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ReadPosRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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European (Finnish)
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ClippingRankSum
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FS
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InbreedingCoeff
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DP
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MQRankSum
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QD
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MQ
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Latino
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.981e1

DP
type: SiteQuality
SIO_000300: 1.26805e6

QD
type: SiteQuality
SIO_000300: 1.408e1

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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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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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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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: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 171
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7196
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 6.009615384615385e-4
allele num: 1664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.004e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.034e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.14e-2

DP
type: SiteQuality
SIO_000300: 4.21048e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.288e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

BaseQRankSum
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SIO_000300: 1.03e0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 12

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9044
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.683501683501683e-3
allele num: 594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7212
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1668
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 4.26995e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.05e-2

QD
type: SiteQuality
SIO_000300: 1.463e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 952
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.023541453428864e-4
allele num: 9770
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.763e1

QD
type: SiteQuality
SIO_000300: 1.264e1

DP
type: SiteQuality
SIO_000300: 4.71104e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.414e0

VQSLOD
type: SiteQuality
SIO_000300: -1.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.51e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.916810427448725e-4
allele num: 10434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1074
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 8.880000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.482e0

DP
type: SiteQuality
SIO_000300: 5.02676e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

FS
type: SiteQuality
SIO_000300: 3.171e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 982
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7866
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1204
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

BaseQRankSum
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SIO_000300: -7.31e-1

MQ
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SIO_000300: 5.203e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-2

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.22718e5

VQSLOD
type: SiteQuality
SIO_000300: -1.025e0

QD
type: SiteQuality
SIO_000300: 1.204e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 428
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1460
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 4.173622704507513e-4
allele num: 2396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13286
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8280
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.28e-2

VQSLOD
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SIO_000300: -1.941e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.929e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.795e0

MQRankSum
type: SiteQuality
SIO_000300: -9.4e-2

DP
type: SiteQuality
SIO_000300: 5.70204e5

MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
type: SiteQuality
SIO_000300: 1.922e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1214
num of homozygotes: 0

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

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1884
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 3.050268423621279e-4
allele num: 16392
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

MQ
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SIO_000300: 5.714e1

MQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

InbreedingCoeff
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SIO_000300: -1.72e-2

QD
type: SiteQuality
SIO_000300: 1.102e1

DP
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SIO_000300: 6.26716e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.108e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.216e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9554
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 23218
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 7.987220447284345e-4
allele num: 2504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3996
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2070
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQ
type: SiteQuality
SIO_000300: 5.763e1

VQSLOD
type: SiteQuality
SIO_000300: -1.338e0

QD
type: SiteQuality
SIO_000300: 1.076e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 7.24943e5

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3238
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29342
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4972
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3492
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.22e-2

MQ
type: SiteQuality
SIO_000300: 5.866e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.411e1

DP
type: SiteQuality
SIO_000300: 8.1198e5

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 1.259445843828715e-4
allele num: 31760
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10590
num of homozygotes: 0

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

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3790
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.78e-1

InbreedingCoeff
type: SiteQuality
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VQSLOD
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MQ
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SIO_000300: 5.968e1

QD
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FS
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MQRankSum
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SIO_000300: 3.37e-1

BaseQRankSum
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SIO_000300: -3.317e0

DP
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.182929491377429e-5
allele num: 45810
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7496
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6432
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

Other
type: Population
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5284
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.099605274208449e-5
allele num: 47628
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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DP
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FS
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BaseQRankSum
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QD
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.040150155051412e-5
allele num: 49016
num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

South Asian
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Latino
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African
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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Latino
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African
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European (Non-Finnish)
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allele num: 53040
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FS
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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QD
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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South Asian
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African
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European (Non-Finnish)
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allele num: 53896
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European (Finnish)
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DP
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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MQ
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DP
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FS
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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South Asian
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East Asian
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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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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European (Finnish)
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Latino
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African
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East Asian
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South Asian
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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FS
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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Other
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South Asian
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European (Finnish)
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African
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQ
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DP
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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VQSLOD
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FS
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DP
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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DP
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ReadPosRankSum
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African
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MQ
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VQSLOD
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FS
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DP
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ClippingRankSum
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bin: 8.75e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.408e0

MQ
type: SiteQuality
SIO_000300: 5.668e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.423094e6

FS
type: SiteQuality
SIO_000300: 8.249000000000001e0

QD
type: SiteQuality
SIO_000300: 1.495e1

VQSLOD
type: SiteQuality
SIO_000300: -2.202e0

MQRankSum
type: SiteQuality
SIO_000300: 8.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.735e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e0

GenotypeDepth
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bin: 6.75e1
variant carriers: 1

GenotypeDepth
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bin: 7.75e1
variant carriers: 2

GenotypeDepth
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bin: 2.5e0
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 5
allele frequency: 5.777675063554426e-4
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.883e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.683e0

DP
type: SiteQuality
SIO_000300: 1.423709e6

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.78e-1

QD
type: SiteQuality
SIO_000300: 1.311e1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
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: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.6882e1

QD
type: SiteQuality
SIO_000300: 2.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

DP
type: SiteQuality
SIO_000300: 1.423652e6

VQSLOD
type: SiteQuality
SIO_000300: -2.236e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.8e0

MQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.796e1

GenotypeDepth
all individuals: 622
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variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 96
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 20
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
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: 10400
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
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SIO_000300: -1.328e0

DP
type: SiteQuality
SIO_000300: 1.424172e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.36e-1

FS
type: SiteQuality
SIO_000300: 1.421e0

VQSLOD
type: SiteQuality
SIO_000300: -3.453e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.126e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.091e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.729804532087874e-4
allele num: 11562
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: 906
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
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BaseQRankSum
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MQ
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ClippingRankSum
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QD
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DP
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SIO_000300: 1.424289e6

MQRankSum
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SIO_000300: 1.41e0

ReadPosRankSum
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SIO_000300: -1.277e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

InbreedingCoeff
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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MQRankSum
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MQ
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BaseQRankSum
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QD
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SIO_000300: 1.091e1

ReadPosRankSum
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