1-6133757-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133757
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133757
    reference: chr 1
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.122-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-38-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.115-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.122-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.263-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.299-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.122-36C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.122-36C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7837
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-6133766-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133766
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133766
    reference: chr 1
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.164-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.122-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.164-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.164-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.164-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.263-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-38-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.115-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.164-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.122-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.164-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.299-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.122-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.122-27A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.164-27A>G
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

1-6133768-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133768
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133768
    reference: chr 1
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.164-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.164-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.164-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.122-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.263-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.164-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.164-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.164-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.122-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-38-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.122-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.164-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.299-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.122-25C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.115-25C>G
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

1-6133776-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133776
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133776
    reference: chr 1
allele count: 2
allele frequency: 1.647880825258717e-5
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.164-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.164-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.122-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.122-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.122-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.122-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-38-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.263-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.164-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.115-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.164-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.164-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.164-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.299-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.164-17C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

1-6133779-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133779
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133779
    reference: chr 1
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.299-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.263-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.164-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.164-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.122-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.122-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.115-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-38-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.164-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.164-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.164-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.122-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.164-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.164-14G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.122-14G>C
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

1-6133782-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133782
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133782
    reference: chr 1
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.164-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.299-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.164-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.164-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.115-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.122-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.164-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.164-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-38-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.122-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.164-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.164-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.122-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.122-11T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.263-11T>C
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

1-6133786-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133786
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133786
    reference: chr 1
allele count: 5
allele frequency: 4.119702063146793e-5
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.122-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.164-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.122-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.164-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.164-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-38-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.164-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.164-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.122-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.122-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.164-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.299-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.263-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.164-7C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.115-7C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.263-7C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

1-6133787-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133787
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133787
    reference: chr 1
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.164-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.164-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.122-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-38-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.115-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.122-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.299-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.164-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.122-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.263-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.164-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.164-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.122-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.164-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.164-6T>C
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.263-6T>C
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

1-6133788-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133788
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133788
    reference: chr 1
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.115-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.263-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.164-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.164-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.164-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.164-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.299-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.122-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-38-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.122-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.164-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.164-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.164-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.122-5T>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.122-5T>A
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.263-5T>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

1-6133789-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133789
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133789
    reference: chr 1
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.115-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.122-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.164-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.164-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.164-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.122-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.164-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.164-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.122-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.122-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-38-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.263-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.164-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.299-4C>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.164-4C>G
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.263-4C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-6133797-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133797
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133797
    reference: chr 1
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.168A>G
  hgvsp: ENST00000164247.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.168A>G
  hgvsp: ENST00000378111.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.119A>G
  hgvsp: ENST00000472700.2:c.119A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.126A>G
  hgvsp: ENST00000378092.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.126A>G
  hgvsp: ENST00000428161.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.126A>G
  hgvsp: ENST00000352527.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.168A>G
  hgvsp: ENST00000389632.4:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.126A>G
  hgvsp: ENST00000435937.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.168A>G
  hgvsp: ENST00000378087.3:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.168A>G
  hgvsp: ENST00000341524.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.267A>G
  hgvsp: ENST00000378083.3:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.168A>G
  hgvsp: ENST00000602612.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.303A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-34A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.168A>G
  hgvsp: ENST00000378097.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr89Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

1-6133809-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133809
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133809
    reference: chr 1
allele count: 20
allele frequency: 1.647989452867502e-4
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.131C>T
  hgvsp: ENST00000472700.2:c.131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.180C>T
  hgvsp: ENST00000389632.4:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.180C>T
  hgvsp: ENST00000341524.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.315C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.138C>T
  hgvsp: ENST00000435937.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.180C>T
  hgvsp: ENST00000378087.3:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.138C>T
  hgvsp: ENST00000428161.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.279C>T
  hgvsp: ENST00000378083.3:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.180C>T
  hgvsp: ENST00000164247.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.180C>T
  hgvsp: ENST00000602612.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.138C>T
  hgvsp: ENST00000378092.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-22C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.180C>T
  hgvsp: ENST00000378097.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.180C>T
  hgvsp: ENST00000378111.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.138C>T
  hgvsp: ENST00000352527.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe93Phe
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

1-6133810-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133810
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133810
    reference: chr 1
allele count: 3
allele frequency: 2.471861971227527e-5
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.181G>A
  hgvsp: ENSP00000340824.1:p.Gly61Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.132G>A
  hgvsp: ENSP00000464860.1:p.Gly45Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.181G>A
  hgvsp: ENSP00000367351.1:p.Gly61Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.139G>A
  hgvsp: ENSP00000367332.1:p.Gly47Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.181G>A
  hgvsp: ENSP00000374283.4:p.Gly61Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.316G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.139G>A
  hgvsp: ENSP00000389151.1:p.Gly47Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.280G>A
  hgvsp: ENSP00000367323.3:p.Gly94Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.181G>A
  hgvsp: ENSP00000367327.3:p.Gly61Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.139G>A
  hgvsp: ENSP00000400285.1:p.Gly47Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.181G>A
  hgvsp: ENSP00000164247.1:p.Gly61Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.181G>A
  hgvsp: ENSP00000473602.1:p.Gly61Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.139G>A
  hgvsp: ENSP00000318772.1:p.Gly47Arg
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.181G>A
  hgvsp: ENSP00000367337.1:p.Gly61Arg
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly94Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum

1-6133826-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133826
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133826
    reference: chr 1
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.296A>G
  hgvsp: ENSP00000367323.3:p.Asp99Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.197A>G
  hgvsp: ENSP00000374283.4:p.Asp66Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.197A>G
  hgvsp: ENSP00000473602.1:p.Asp66Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.197A>G
  hgvsp: ENSP00000367337.1:p.Asp66Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.155A>G
  hgvsp: ENSP00000400285.1:p.Asp52Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.155A>G
  hgvsp: ENSP00000367332.1:p.Asp52Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-5A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.197A>G
  hgvsp: ENSP00000164247.1:p.Asp66Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.155A>G
  hgvsp: ENSP00000318772.1:p.Asp52Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.155A>G
  hgvsp: ENSP00000389151.1:p.Asp52Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.148A>G
  hgvsp: ENSP00000464860.1:p.Asp50Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.197A>G
  hgvsp: ENSP00000367327.3:p.Asp66Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.197A>G
  hgvsp: ENSP00000367351.1:p.Asp66Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.332A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.197A>G
  hgvsp: ENSP00000340824.1:p.Asp66Gly
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp99Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

1-6133829-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133829
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133830
    reference: chr 1
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.201+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.159+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.300+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.201+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-1+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.201+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.159+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.337dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.201+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.159+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.201+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.152+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.159+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.201+1dupG
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.201+1dupG
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 6895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-6133837-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133837
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133837
    reference: chr 1
allele count: 3
allele frequency: 2.472513887286333e-5
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.201+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.300+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.159+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.201+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.159+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.201+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.343T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.152+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.201+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-1+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.159+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.201+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.201+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.201+7T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.159+7T>C
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.300+7T>C
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

1-6133869-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133869
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133869
    reference: chr 1
allele count: 2
allele frequency: 1.650273945474949e-5
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.201+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.201+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.152+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.159+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.375G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.300+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.201+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.201+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.159+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.201+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.159+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-1+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.159+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.201+39G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.201+39G>A
  variant of: http://identifiers.org/hgnc/6229
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6819
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

1-6133870-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133870
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133870
    reference: chr 1
allele count: 2043
allele frequency: 1.685699197993333e-2
allele num: 121196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.201+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.159+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.201+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.201+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.152+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.201+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.201+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.159+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.300+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.201+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.376G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-1+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.159+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.201+40G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.159+40G>A
  variant of: http://identifiers.org/hgnc/6229
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 8.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8059
  bin: 4.75e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 5.75e1
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 8.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 6.25e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 7.25e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 3.75e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7231
  bin: 5.25e1
  variant carriers: 173
genotype quality: GenotypeQuality
num of homozygotes: 168
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum

1-6133871-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133871
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133871
    reference: chr 1
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.152+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.201+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.377G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.201+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.201+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.300+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.201+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-1+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.159+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.201+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.159+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.201+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.201+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.159+41G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.159+41G>T
  variant of: http://identifiers.org/hgnc/6229
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6851
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5900
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-6133875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6133875
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6133875
    reference: chr 1
allele count: 23
allele frequency: 1.898159610464637e-4
allele num: 121170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.159+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.201+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.-1+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.300+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000069424
  ensembl transcript: ENST00000478098
  gene symbol: KCNAB2
  hgvsc: ENST00000478098.1:n.381G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.159+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.159+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.152+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.201+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.201+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.159+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.201+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.201+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.201+45G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.201+45G>A
  variant of: http://identifiers.org/hgnc/6229
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5898
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7872
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

1-6142220-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142220
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142220
    reference: chr 1
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.202-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.160-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.202-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.160-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.202-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.202-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.160-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.202-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.301-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.153-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.202-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.160-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.202-35C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.1-35C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5096
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-6142221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142221
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142221
    reference: chr 1
allele count: 99
allele frequency: 8.165083135391924e-4
allele num: 121248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.1-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.202-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.202-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.160-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.202-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.202-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.160-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.301-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.202-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.153-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.202-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.202-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.160-34G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.160-34G>A
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6379
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7106
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

1-6142232-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142232
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142232
    reference: chr 1
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.202-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.153-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.1-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.160-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.301-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.160-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.202-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.202-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.202-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.202-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.160-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.202-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.202-23C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.160-23C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5092
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/1-6142233-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142233
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142233
    reference: chr 1
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.160-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.160-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.202-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.202-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.301-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.202-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.153-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.202-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.202-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.160-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.1-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.160-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.202-22A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.202-22A>C
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

1-6142238-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142238
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142238
    reference: chr 1
allele count: 6
allele frequency: 4.950658437572197e-5
allele num: 121196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.202-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.202-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.160-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.160-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.153-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.202-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.301-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.160-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.202-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.202-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.202-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.160-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.202-17C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.1-17C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7377
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

1-6142241-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142241
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142241
    reference: chr 1
allele count: 81
allele frequency: 6.726122265955857e-4
allele num: 120426
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.301-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.202-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.160-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.202-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.202-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.153-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.202-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.160-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.202-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.202-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.160-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.1-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.160-14T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.202-14T>G
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7335
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6568
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 6.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

1-6142245-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142245
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142245
    reference: chr 1
allele count: 2
allele frequency: 1.648695881557688e-5
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.202-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.160-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.1-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.153-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.301-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.202-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.202-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.202-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.202-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.202-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.202-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.160-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.160-10C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.160-10C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

1-6142247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142247
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142247
    reference: chr 1
allele count: 6
allele frequency: 4.944212798918866e-5
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.160-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.160-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.202-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.202-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.301-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.202-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.202-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.202-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.160-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.202-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.1-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.160-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.202-8C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.153-8C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.301-8C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

1-6142248-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142248
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142248
    reference: chr 1
allele count: 11
allele frequency: 9.06409136604097e-5
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.202-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.202-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.1-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.153-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.202-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.202-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.202-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.202-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.160-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.301-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.160-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.202-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.160-7G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.160-7G>A
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7054
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.301-7G>A
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

1-6142251-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142251
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142251
    reference: chr 1
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.160-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.1-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.160-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.160-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.202-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.202-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.202-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.153-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.301-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.202-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.202-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.202-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.160-4T>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.202-4T>G
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.301-4T>G
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

1-6142257-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142257
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142257
    reference: chr 1
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.162G>A
  hgvsp: ENSP00000367332.1:p.Met54Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.204G>A
  hgvsp: ENSP00000374283.4:p.Met68Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.204G>A
  hgvsp: ENSP00000473602.1:p.Met68Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.162G>A
  hgvsp: ENSP00000318772.1:p.Met54Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.155G>A
  hgvsp: ENSP00000464860.1:p.Met52Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.204G>A
  hgvsp: ENSP00000367327.3:p.Met68Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.3G>A
  hgvsp: ENSP00000396167.2:p.Met1?
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.303G>A
  hgvsp: ENSP00000367323.3:p.Met101Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.204G>A
  hgvsp: ENSP00000367337.1:p.Met68Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.162G>A
  hgvsp: ENSP00000389151.1:p.Met54Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.162G>A
  hgvsp: ENSP00000400285.1:p.Met54Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.204G>A
  hgvsp: ENSP00000164247.1:p.Met68Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.204G>A
  hgvsp: ENSP00000340824.1:p.Met68Ile
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.204G>A
  hgvsp: ENSP00000367351.1:p.Met68Ile
  variant of: http://identifiers.org/hgnc/6229
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

1-6142263-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142263
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142263
    reference: chr 1
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.9G>A
  hgvsp: ENST00000458166.2:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.210G>A
  hgvsp: ENST00000378111.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.309G>A
  hgvsp: ENST00000378083.3:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.210G>A
  hgvsp: ENST00000378097.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.161G>A
  hgvsp: ENST00000472700.2:c.161G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.210G>A
  hgvsp: ENST00000378087.3:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.168G>A
  hgvsp: ENST00000352527.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.168G>A
  hgvsp: ENST00000378092.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.168G>A
  hgvsp: ENST00000428161.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.210G>A
  hgvsp: ENST00000602612.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.210G>A
  hgvsp: ENST00000341524.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.168G>A
  hgvsp: ENST00000435937.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.210G>A
  hgvsp: ENST00000389632.4:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.210G>A
  hgvsp: ENST00000164247.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu103Glu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/1-6142274-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142274
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142274
    reference: chr 1
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.221C>A
  hgvsp: ENSP00000367337.1:p.Thr74Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.221C>A
  hgvsp: ENSP00000374283.4:p.Thr74Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.221C>A
  hgvsp: ENSP00000367351.1:p.Thr74Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.320C>A
  hgvsp: ENSP00000367323.3:p.Thr107Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.20C>A
  hgvsp: ENSP00000396167.2:p.Thr7Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.221C>A
  hgvsp: ENSP00000164247.1:p.Thr74Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.179C>A
  hgvsp: ENSP00000400285.1:p.Thr60Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.179C>A
  hgvsp: ENSP00000389151.1:p.Thr60Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.221C>A
  hgvsp: ENSP00000473602.1:p.Thr74Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.179C>A
  hgvsp: ENSP00000367332.1:p.Thr60Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.172C>A
  hgvsp: ENSP00000464860.1:p.Thr58Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.221C>A
  hgvsp: ENSP00000367327.3:p.Thr74Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.221C>A
  hgvsp: ENSP00000340824.1:p.Thr74Asn
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.179C>A
  hgvsp: ENSP00000318772.1:p.Thr60Asn
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7060
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr107Asn
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

1-6142278-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142278
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142278
    reference: chr 1
allele count: 3
allele frequency: 2.471128976458378e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.183G>A
  hgvsp: ENST00000378092.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.225G>A
  hgvsp: ENST00000378111.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.183G>A
  hgvsp: ENST00000435937.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.24G>A
  hgvsp: ENST00000458166.2:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.176G>A
  hgvsp: ENST00000472700.2:c.176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.225G>A
  hgvsp: ENST00000378097.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.225G>A
  hgvsp: ENST00000389632.4:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.183G>A
  hgvsp: ENST00000352527.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.225G>A
  hgvsp: ENST00000164247.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.225G>A
  hgvsp: ENST00000602612.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.324G>A
  hgvsp: ENST00000378083.3:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.225G>A
  hgvsp: ENST00000341524.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.225G>A
  hgvsp: ENST00000378087.3:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.183G>A
  hgvsp: ENST00000428161.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7061
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu108Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

1-6142305-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142305
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142305
    reference: chr 1
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.252C>T
  hgvsp: ENST00000378097.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.51C>T
  hgvsp: ENST00000458166.2:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.210C>T
  hgvsp: ENST00000428161.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.252C>T
  hgvsp: ENST00000378087.3:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.210C>T
  hgvsp: ENST00000352527.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.252C>T
  hgvsp: ENST00000389632.4:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.252C>T
  hgvsp: ENST00000378111.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.210C>T
  hgvsp: ENST00000435937.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.252C>T
  hgvsp: ENST00000164247.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.351C>T
  hgvsp: ENST00000378083.3:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.203C>T
  hgvsp: ENST00000472700.2:c.203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.210C>T
  hgvsp: ENST00000378092.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.252C>T
  hgvsp: ENST00000602612.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.252C>T
  hgvsp: ENST00000341524.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe117Phe
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

1-6142308-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142308
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142308
    reference: chr 1
allele count: 10907
allele frequency: 8.984201248743842e-2
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.206T>C
  hgvsp: ENST00000472700.2:c.206T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.213T>C
  hgvsp: ENST00000352527.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.255T>C
  hgvsp: ENST00000378111.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.54T>C
  hgvsp: ENST00000458166.2:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.255T>C
  hgvsp: ENST00000389632.4:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.213T>C
  hgvsp: ENST00000428161.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.213T>C
  hgvsp: ENST00000435937.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.354T>C
  hgvsp: ENST00000378083.3:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.255T>C
  hgvsp: ENST00000378087.3:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.255T>C
  hgvsp: ENST00000602612.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.255T>C
  hgvsp: ENST00000341524.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.255T>C
  hgvsp: ENST00000164247.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.255T>C
  hgvsp: ENST00000378097.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.213T>C
  hgvsp: ENST00000378092.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 7.75e1
  variant carriers: 223
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 6.25e1
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 5.75e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 6616
  bin: 4.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 5.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 6.75e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 8.75e1
  variant carriers: 287
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 7.25e1
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 2.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
hgvs: p.Asp118Asp
num of homozygotes: 606
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

1-6142313-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142313
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142313
    reference: chr 1
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.260C>G
  hgvsp: ENSP00000374283.4:p.Ala87Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.59C>G
  hgvsp: ENSP00000396167.2:p.Ala20Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.218C>G
  hgvsp: ENSP00000400285.1:p.Ala73Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.218C>G
  hgvsp: ENSP00000367332.1:p.Ala73Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.260C>G
  hgvsp: ENSP00000367337.1:p.Ala87Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.218C>G
  hgvsp: ENSP00000318772.1:p.Ala73Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.260C>G
  hgvsp: ENSP00000164247.1:p.Ala87Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.260C>G
  hgvsp: ENSP00000473602.1:p.Ala87Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.260C>G
  hgvsp: ENSP00000367327.3:p.Ala87Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.211C>G
  hgvsp: ENSP00000464860.1:p.Ala71Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.260C>G
  hgvsp: ENSP00000367351.1:p.Ala87Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.260C>G
  hgvsp: ENSP00000340824.1:p.Ala87Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.218C>G
  hgvsp: ENSP00000389151.1:p.Ala73Gly
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.359C>G
  hgvsp: ENSP00000367323.3:p.Ala120Gly
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala120Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/1-6142316-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142316
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142316
    reference: chr 1
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.221A>C
  hgvsp: ENSP00000389151.1:p.Glu74Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.62A>C
  hgvsp: ENSP00000396167.2:p.Glu21Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.263A>C
  hgvsp: ENSP00000340824.1:p.Glu88Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.221A>C
  hgvsp: ENSP00000400285.1:p.Glu74Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.263A>C
  hgvsp: ENSP00000374283.4:p.Glu88Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.362A>C
  hgvsp: ENSP00000367323.3:p.Glu121Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.263A>C
  hgvsp: ENSP00000164247.1:p.Glu88Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.263A>C
  hgvsp: ENSP00000367351.1:p.Glu88Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.263A>C
  hgvsp: ENSP00000473602.1:p.Glu88Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.221A>C
  hgvsp: ENSP00000318772.1:p.Glu74Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.263A>C
  hgvsp: ENSP00000367327.3:p.Glu88Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.214A>C
  hgvsp: ENSP00000464860.1:p.Glu72Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.221A>C
  hgvsp: ENSP00000367332.1:p.Glu74Ala
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.263A>C
  hgvsp: ENSP00000367337.1:p.Glu88Ala
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu121Ala
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

1-6142323-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142323
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142323
    reference: chr 1
allele count: 6
allele frequency: 4.942583653228331e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.228C>T
  hgvsp: ENST00000352527.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.369C>T
  hgvsp: ENST00000378083.3:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.270C>T
  hgvsp: ENST00000602612.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.270C>T
  hgvsp: ENST00000164247.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.270C>T
  hgvsp: ENST00000378097.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.228C>T
  hgvsp: ENST00000378092.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.69C>T
  hgvsp: ENST00000458166.2:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.3C>T
  hgvsp: ENST00000462676.2:c.3C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.221C>T
  hgvsp: ENST00000472700.2:c.221C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.270C>T
  hgvsp: ENST00000389632.4:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.270C>T
  hgvsp: ENST00000378111.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.270C>T
  hgvsp: ENST00000341524.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.270C>T
  hgvsp: ENST00000378087.3:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.228C>T
  hgvsp: ENST00000435937.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.228C>T
  hgvsp: ENST00000428161.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7705
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr123Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

1-6142324-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142324
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142324
    reference: chr 1
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.229G>A
  hgvsp: ENSP00000400285.1:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.271G>A
  hgvsp: ENSP00000367337.1:p.Ala91Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.271G>A
  hgvsp: ENSP00000367351.1:p.Ala91Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.271G>A
  hgvsp: ENSP00000367327.3:p.Ala91Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.4G>A
  hgvsp: ENSP00000465785.1:p.Ala2Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.271G>A
  hgvsp: ENSP00000374283.4:p.Ala91Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.370G>A
  hgvsp: ENSP00000367323.3:p.Ala124Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.229G>A
  hgvsp: ENSP00000389151.1:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.222G>A
  hgvsp: ENSP00000464860.1:p.Ala75Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.271G>A
  hgvsp: ENSP00000164247.1:p.Ala91Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.271G>A
  hgvsp: ENSP00000473602.1:p.Ala91Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.70G>A
  hgvsp: ENSP00000396167.2:p.Ala24Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.229G>A
  hgvsp: ENSP00000318772.1:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.271G>A
  hgvsp: ENSP00000340824.1:p.Ala91Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.229G>A
  hgvsp: ENSP00000367332.1:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala124Thr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

1-6142327-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142327
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142327
    reference: chr 1
allele count: 4
allele frequency: 3.295327225993541e-5
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.274G>A
  hgvsp: ENSP00000374283.4:p.Ala92Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.232G>A
  hgvsp: ENSP00000389151.1:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.274G>A
  hgvsp: ENSP00000340824.1:p.Ala92Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.7G>A
  hgvsp: ENSP00000465785.1:p.Ala3Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.232G>A
  hgvsp: ENSP00000367332.1:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.232G>A
  hgvsp: ENSP00000400285.1:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.274G>A
  hgvsp: ENSP00000367351.1:p.Ala92Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.274G>A
  hgvsp: ENSP00000473602.1:p.Ala92Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.274G>A
  hgvsp: ENSP00000367337.1:p.Ala92Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.73G>A
  hgvsp: ENSP00000396167.2:p.Ala25Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.274G>A
  hgvsp: ENSP00000164247.1:p.Ala92Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.373G>A
  hgvsp: ENSP00000367323.3:p.Ala125Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.225G>A
  hgvsp: ENSP00000464860.1:p.Ala76Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.232G>A
  hgvsp: ENSP00000318772.1:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.274G>A
  hgvsp: ENSP00000367327.3:p.Ala92Thr
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala125Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

1-6142329-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142329
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142329
    reference: chr 1
allele count: 1522
allele frequency: 1.253851350238083e-2
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.234C>T
  hgvsp: ENST00000428161.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.276C>T
  hgvsp: ENST00000378087.3:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.276C>T
  hgvsp: ENST00000341524.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.9C>T
  hgvsp: ENST00000462676.2:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.234C>T
  hgvsp: ENST00000352527.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.276C>T
  hgvsp: ENST00000378097.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.276C>T
  hgvsp: ENST00000378111.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.227C>T
  hgvsp: ENST00000472700.2:c.227C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.276C>T
  hgvsp: ENST00000164247.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.375C>T
  hgvsp: ENST00000378083.3:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.75C>T
  hgvsp: ENST00000458166.2:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.276C>T
  hgvsp: ENST00000389632.4:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.276C>T
  hgvsp: ENST00000602612.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.234C>T
  hgvsp: ENST00000435937.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.234C>T
  hgvsp: ENST00000378092.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7203
  bin: 4.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 7438
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7647
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
hgvs: p.Ala125Ala
num of homozygotes: 101
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

1-6142330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142330
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142330
    reference: chr 1
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.277G>A
  hgvsp: ENSP00000367351.1:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.277G>A
  hgvsp: ENSP00000367327.3:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.235G>A
  hgvsp: ENSP00000389151.1:p.Gly79Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.235G>A
  hgvsp: ENSP00000400285.1:p.Gly79Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.277G>A
  hgvsp: ENSP00000374283.4:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.10G>A
  hgvsp: ENSP00000465785.1:p.Gly4Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.277G>A
  hgvsp: ENSP00000340824.1:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.277G>A
  hgvsp: ENSP00000473602.1:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.76G>A
  hgvsp: ENSP00000396167.2:p.Gly26Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.235G>A
  hgvsp: ENSP00000367332.1:p.Gly79Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.277G>A
  hgvsp: ENSP00000367337.1:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.376G>A
  hgvsp: ENSP00000367323.3:p.Gly126Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.235G>A
  hgvsp: ENSP00000318772.1:p.Gly79Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.277G>A
  hgvsp: ENSP00000164247.1:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.228G>A
  hgvsp: ENSP00000464860.1:p.Gly77Ser
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6255
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly126Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-6142341-GTCTTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142341
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142336
    reference: chr 1
allele count: 1563
allele frequency: 1.287797643569251e-2
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.281+10_281+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.281+10_281+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.80+10_80+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.14+10_14+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.281+10_281+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.380+10_380+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.281+10_281+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.281+10_281+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.281+10_281+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.232+10_232+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.281+10_281+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.239+10_239+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.239+10_239+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.239+10_239+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.239+10_239+14delTTTTC
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 4.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 3.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 3.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 9.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6276
  bin: 5.25e1
  variant carriers: 93
genotype quality: GenotypeQuality
hgvs: c.380+10_380+14delTTTTC
num of homozygotes: 105
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: GTCTTT
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

1-6142352-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142352
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142352
    reference: chr 1
allele count: 9
allele frequency: 7.417297136923305e-5
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.281+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.281+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.239+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.239+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.380+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.281+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.239+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.281+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.281+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.232+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.281+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.281+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.239+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.14+18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.80+18C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

1-6142353-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142353
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142353
    reference: chr 1
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.281+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.239+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.281+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.14+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.281+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.380+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.281+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.239+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.239+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.232+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.281+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.239+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.281+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.281+19G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.80+19G>A
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-6142355-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142355
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142356
    reference: chr 1
allele count: 6
allele frequency: 4.945190801945108e-5
allele num: 121330
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.239+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.281+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.380+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.281+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.232+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.239+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.281+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.239+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.281+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.281+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.14+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.281+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.80+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.281+26dupA
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.239+26dupA
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-6142357-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142357
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142357
    reference: chr 1
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.80+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.281+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.281+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.232+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.281+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.380+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.239+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.281+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.281+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.281+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.14+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.281+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.239+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.239+23A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.239+23A>C
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-6142358-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142358
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142358
    reference: chr 1
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.232+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.281+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.380+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.281+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.281+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.281+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.14+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.239+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.239+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.239+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.281+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.281+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.239+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.80+24A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.281+24A>G
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7854
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-6142360-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142360
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142360
    reference: chr 1
allele count: 685
allele frequency: 5.646038706274109e-3
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.281+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.281+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.281+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.380+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.281+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.239+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.281+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.14+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.281+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.80+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.239+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.232+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.281+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.239+26A>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.239+26A>C
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 8.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 7556
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 7931
  bin: 4.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 6.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 7.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 8.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 6.75e1
  variant carriers: 49
genotype quality: GenotypeQuality
num of homozygotes: 15
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-6142370-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142370
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142370
    reference: chr 1
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.281+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.380+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.239+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.281+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.281+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.232+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.14+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.281+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.239+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.281+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.239+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.239+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.281+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.80+36A>G
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.281+36A>G
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6286
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-6142378-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142378
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142378
    reference: chr 1
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.281+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.239+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.281+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.281+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.281+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.281+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.380+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.281+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.14+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.239+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.232+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.239+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.80+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.239+44G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.281+44G>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

1-6142386-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6142386
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6142386
    reference: chr 1
allele count: 1
allele frequency: 8.258456659619451e-6
allele num: 121088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.281+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.80+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.14+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.281+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.380+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.239+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.239+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.281+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.281+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.232+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.281+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.281+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.239+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.239+52C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.281+52C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4870
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

1-6145217-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145217
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145217
    reference: chr 1
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-47G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-47G>C
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8405
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

1-6145221-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145221
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145221
    reference: chr 1
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-43T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-43T>C
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

1-6145232-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145232
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145232
    reference: chr 1
allele count: 9
allele frequency: 7.414486258485467e-5
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-32C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-32C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5186
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-6145241-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145241
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145241
    reference: chr 1
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-23G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-23G>A
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

1-6145243-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145243
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145243
    reference: chr 1
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-21G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-21G>A
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

1-6145243-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145243
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145243
    reference: chr 1
allele count: 3
allele frequency: 2.471413978317461e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-21G>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-21G>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8406
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5186
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

1-6145244-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145244
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145244
    reference: chr 1
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-20C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-20C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

1-6145246-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145246
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145246
    reference: chr 1
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-18C>T
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-18C>T
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

1-6145247-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145247
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145247
    reference: chr 1
allele count: 7
allele frequency: 5.766537606063102e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-17G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-17G>A
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

1-6145248-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145248
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145248
    reference: chr 1
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-16G>A
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-16G>A
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

1-6145255-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145255
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145255
    reference: chr 1
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-9G>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-9G>C
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

1-6145258-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6145258
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6145258
    reference: chr 1
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000340824
  ensembl transcript: ENST00000341524
  gene symbol: KCNAB2
  hgvsc: ENST00000341524.1:c.282-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000396167
  ensembl transcript: ENST00000458166
  gene symbol: KCNAB2
  hgvsc: ENST00000458166.2:c.81-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367351
  ensembl transcript: ENST00000378111
  gene symbol: KCNAB2
  hgvsc: ENST00000378111.1:c.282-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000389151
  ensembl transcript: ENST00000435937
  gene symbol: KCNAB2
  hgvsc: ENST00000435937.1:c.240-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000473602
  ensembl transcript: ENST00000602612
  gene symbol: KCNAB2
  hgvsc: ENST00000602612.1:c.282-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367327
  ensembl transcript: ENST00000378087
  gene symbol: KCNAB2
  hgvsc: ENST00000378087.3:c.282-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000400285
  ensembl transcript: ENST00000428161
  gene symbol: KCNAB2
  hgvsc: ENST00000428161.1:c.240-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000164247
  ensembl transcript: ENST00000164247
  gene symbol: KCNAB2
  hgvsc: ENST00000164247.1:c.282-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367323
  ensembl transcript: ENST00000378083
  gene symbol: KCNAB2
  hgvsc: ENST00000378083.3:c.381-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000318772
  ensembl transcript: ENST00000352527
  gene symbol: KCNAB2
  hgvsc: ENST00000352527.1:c.240-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367332
  ensembl transcript: ENST00000378092
  gene symbol: KCNAB2
  hgvsc: ENST00000378092.1:c.240-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000464860
  ensembl transcript: ENST00000472700
  gene symbol: KCNAB2
  hgvsc: ENST00000472700.2:c.233-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000465785
  ensembl transcript: ENST00000462676
  gene symbol: KCNAB2
  hgvsc: ENST00000462676.2:c.15-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000374283
  ensembl transcript: ENST00000389632
  gene symbol: KCNAB2
  hgvsc: ENST00000389632.4:c.282-6T>C
  variant of: http://identifiers.org/hgnc/6229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069424
  ensembl protein: ENSP00000367337
  ensembl transcript: ENST00000378097
  gene symbol: KCNAB2
  hgvsc: ENST00000378097.1:c.282-6T>C
  variant of: http://identifiers.org/hgnc/6229
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8403
  bin: 9.75e1
  variant carriers: 1
hgvs: c.381-6T>C
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3807
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1259
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4302
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 718
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6900
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8062
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41938
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3454
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2717
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2431
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2886
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.081e1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.500000000000001e-2

FS
type: SiteQuality
SIO_000300: 6.647e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

DP
type: SiteQuality
SIO_000300: 3.019128e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.11e-1

GenotypeDepth
all individuals: 7836
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 717
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6900
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2141
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1066
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 426
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3017
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7226
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2722
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1821
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3737
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2887
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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South Asian
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FS
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InbreedingCoeff
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MQ
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QD
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VQSLOD
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BaseQRankSum
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DP
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MQRankSum
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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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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: 66706
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Latino
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South Asian
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European (Finnish)
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East Asian
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African
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Other
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InbreedingCoeff
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QD
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DP
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FS
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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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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BaseQRankSum
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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VQSLOD
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Latino
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East Asian
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African
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Other
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MQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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FS
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ClippingRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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Other
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DP
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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BaseQRankSum
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GenotypeQuality
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allele frequency: 0.0e0
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East Asian
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Latino
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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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European (Non-Finnish)
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DP
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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VQSLOD
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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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GenotypeQuality
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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African
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DP
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QD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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BaseQRankSum
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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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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: 66710
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South Asian
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African
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Other
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East Asian
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Latino
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num of homozygotes: 0

European (Finnish)
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DP
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SIO_000300: 3.019705e6

VQSLOD
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MQRankSum
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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South Asian
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European (Finnish)
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East Asian
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Other
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European (Non-Finnish)
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allele num: 66704
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VQSLOD
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MQ
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DP
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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Other
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African
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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DP
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MQ
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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African
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European (Finnish)
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South Asian
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Other
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QD
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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MQ
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FS
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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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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

Other
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QD
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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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 frequency: 0.0e0
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num of homozygotes: 0

Other
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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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East Asian
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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 num: 66688
num of homozygotes: 0

South Asian
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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DP
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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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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Latino
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allele frequency: 2.592016588906169e-4
allele num: 11574
num of homozygotes: 0

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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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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South Asian
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num of homozygotes: 0

Other
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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DP
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VQSLOD
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QD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 3.5e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 16510
num of homozygotes: 0

Other
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allele count: 1
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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African
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East Asian
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FS
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VQSLOD
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MQ
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QD
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DP
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 15

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

European (Non-Finnish)
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East Asian
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African
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Other
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DP
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MQRankSum
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InbreedingCoeff
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QD
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FS
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VQSLOD
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BaseQRankSum
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MQ
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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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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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num of homozygotes: 0

Latino
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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DP
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QD
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MQ
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
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allele frequency: 3.469812630117973e-4
allele num: 8646
num of homozygotes: 0

African
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allele frequency: 8.179368745188606e-3
allele num: 10392
num of homozygotes: 0

Latino
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allele frequency: 6.048038707447727e-4
allele num: 11574
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Other
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South Asian
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European (Non-Finnish)
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
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VQSLOD
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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African
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South Asian
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allele num: 16512
num of homozygotes: 0

European (Finnish)
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ClippingRankSum
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MQRankSum
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MQ
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DP
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

Latino
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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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African
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Other
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East Asian
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ClippingRankSum
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VQSLOD
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MQ
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MQRankSum
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DP
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 4

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

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num of homozygotes: 0

European (Non-Finnish)
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Other
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East Asian
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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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InbreedingCoeff
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FS
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DP
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MQRankSum
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ClippingRankSum
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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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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 frequency: 7.8509526829121e-4
allele num: 66234
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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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South Asian
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European (Finnish)
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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FS
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Non-Finnish)
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African
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Latino
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East Asian
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European (Finnish)
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FS
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ClippingRankSum
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VQSLOD
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DP
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QD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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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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African
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Latino
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Other
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South Asian
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East Asian
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European (Non-Finnish)
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VQSLOD
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DP
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 10402
num of homozygotes: 0

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66690
num of homozygotes: 0

Latino
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South Asian
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East Asian
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MQ
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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QD
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VQSLOD
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Other
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African
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European (Non-Finnish)
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Latino
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South Asian
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MQ
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VQSLOD
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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African
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QD
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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ReadPosRankSum
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MQRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

Other
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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
allele num: 16512
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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FS
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BaseQRankSum
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QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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VQSLOD
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 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: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
num of homozygotes: 0

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

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

VQSLOD
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SIO_000300: 8.95e-1

ReadPosRankSum
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FS
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InbreedingCoeff
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MQ
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ClippingRankSum
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DP
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BaseQRankSum
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 2.753e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.37e-1

BaseQRankSum
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SIO_000300: 3.08e0

VQSLOD
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SIO_000300: 1.71e0

MQRankSum
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SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.364e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.03e-1

InbreedingCoeff
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.962491e6

GenotypeDepth
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variant carriers: 33

GenotypeDepth
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variant carriers: 252

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 60

GenotypeDepth
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variant carriers: 8

GenotypeDepth
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GenotypeDepth
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variant carriers: 8311

GenotypeDepth
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variant carriers: 39

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10296

GenotypeQuality
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variant carriers: 0

Latino
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allele count: 455
allele frequency: 3.93054595715273e-2
allele num: 11576
num of homozygotes: 6

South Asian
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allele count: 1376
allele frequency: 8.333333333333333e-2
allele num: 16512
num of homozygotes: 63

Other
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allele count: 93
allele frequency: 1.024229074889868e-1
allele num: 908
num of homozygotes: 4

European (Non-Finnish)
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allele count: 6255
allele frequency: 9.373314152130911e-2
allele num: 66732
num of homozygotes: 308

European (Finnish)
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allele count: 673
allele frequency: 1.017538554581191e-1
allele num: 6614
num of homozygotes: 39

African
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allele count: 2048
allele frequency: 1.968095329617528e-1
allele num: 10406
num of homozygotes: 186

East Asian
type: Population
allele count: 7
allele frequency: 8.088745088976196e-4
allele num: 8654
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -3.62e-1

DP
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InbreedingCoeff
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SIO_000300: 2.28e-2

BaseQRankSum
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MQ
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SIO_000300: 5.956e1

ReadPosRankSum
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SIO_000300: 4.59e-1

FS
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SIO_000300: 0.0e0

MQRankSum
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VQSLOD
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QD
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SIO_000300: 1.502e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele num: 11578
num of homozygotes: 0

South 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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num of homozygotes: 0

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

East Asian
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European (Non-Finnish)
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allele count: 1
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allele num: 66728
num of homozygotes: 0

Other
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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QD
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

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

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

Latino
type: Population
allele count: 5
allele frequency: 4.318535152876144e-4
allele num: 11578
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.949e1

DP
type: SiteQuality
SIO_000300: 2.862519e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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SIO_000300: 1.182e1

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: 3.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.49e-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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 3
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.84e-1

DP
type: SiteQuality
SIO_000300: 2.862094e6

QD
type: SiteQuality
SIO_000300: 1.288e1

FS
type: SiteQuality
SIO_000300: 2.748e0

MQRankSum
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SIO_000300: 1.8e0

VQSLOD
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SIO_000300: -2.633e-1

BaseQRankSum
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SIO_000300: -3.838e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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: 3

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
all individuals: 3
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GenotypeQuality
all individuals: 23
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variant carriers: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

DP
type: SiteQuality
SIO_000300: 2.862353e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.64e0

QD
type: SiteQuality
SIO_000300: 1.343e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.793e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 6222
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variant carriers: 37

GenotypeDepth
all individuals: 1256
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variant carriers: 82

GenotypeDepth
all individuals: 563
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variant carriers: 87

GenotypeDepth
all individuals: 5360
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variant carriers: 4

GenotypeDepth
all individuals: 3594
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GenotypeDepth
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variant carriers: 81

GenotypeDepth
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GenotypeDepth
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variant carriers: 64

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
all individuals: 3300
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 35720
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variant carriers: 1420

African
type: Population
allele count: 1365
allele frequency: 1.311743225062464e-1
allele num: 10406
num of homozygotes: 100

Latino
type: Population
allele count: 79
allele frequency: 6.823285541544308e-3
allele num: 11578
num of homozygotes: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 1.453488372093023e-3
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 43
allele frequency: 6.445230529408237e-4
allele num: 66716
num of homozygotes: 0

Other
type: Population
allele count: 9
allele frequency: 9.911894273127754e-3
allele num: 908
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.974e0

VQSLOD
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SIO_000300: 3.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.223e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

MQ
type: SiteQuality
SIO_000300: 5.169e1

DP
type: SiteQuality
SIO_000300: 2.910944e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.73e-1

FS
type: SiteQuality
SIO_000300: 3.029e0

QD
type: SiteQuality
SIO_000300: 1.374e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.48e0

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
all individuals: 6
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 2089
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GenotypeQuality
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GenotypeQuality
all individuals: 7095
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.511e0

QD
type: SiteQuality
SIO_000300: 3.469e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.89081e6

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.792e0

GenotypeDepth
all individuals: 45
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variant carriers: 5

GenotypeDepth
all individuals: 7789
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variant carriers: 56

GenotypeDepth
all individuals: 1946
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variant carriers: 129

GenotypeDepth
all individuals: 0
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GenotypeDepth
all individuals: 5328
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GenotypeDepth
all individuals: 4862
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GenotypeDepth
all individuals: 1283
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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
all individuals: 1
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 2006
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 5
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GenotypeQuality
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GenotypeQuality
all individuals: 62
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 6903
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 3291
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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variant carriers: 1452

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 22
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variant carriers: 0

African
type: Population
allele count: 1406
allele frequency: 1.351923076923077e-1
allele num: 10400
num of homozygotes: 104

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

South Asian
type: Population
allele count: 25
allele frequency: 1.514050387596899e-3
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 79
allele frequency: 6.824464409122322e-3
allele num: 11576
num of homozygotes: 1

Other
type: Population
allele count: 9
allele frequency: 9.911894273127754e-3
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 42
allele frequency: 6.295907660020986e-4
allele num: 66710
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.036e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.238e-1

FS
type: SiteQuality
SIO_000300: 6.248e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.15e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.203e0

DP
type: SiteQuality
SIO_000300: 2.881459e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.41e-1

ReadPosRankSum
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SIO_000300: 2.19e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

African
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allele count: 5
allele frequency: 4.813246053138236e-4
allele num: 10388
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
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SIO_000300: 9.29e-1

MQ
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VQSLOD
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ClippingRankSum
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SIO_000300: -1.5e-2

MQRankSum
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BaseQRankSum
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DP
type: SiteQuality
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QD
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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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

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

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.837e0

DP
type: SiteQuality
SIO_000300: 2.826237e6

QD
type: SiteQuality
SIO_000300: 1.797e1

VQSLOD
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SIO_000300: 1.12e-1

MQRankSum
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SIO_000300: -3.68e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.23e-1

ClippingRankSum
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SIO_000300: 1.6e0

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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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 6
allele frequency: 6.938020351526364e-4
allele num: 8648
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.6e-1

QD
type: SiteQuality
SIO_000300: 1.186e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e-2

MQRankSum
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SIO_000300: 8.2e-2

ClippingRankSum
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SIO_000300: -4.35e-1

VQSLOD
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.978e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.67e-1

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

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

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

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -1.841e-1

DP
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
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ClippingRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

BaseQRankSum
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SIO_000300: 4.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

South Asian
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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

Latino
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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QD
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 50

GenotypeDepth
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variant carriers: 55

GenotypeDepth
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variant carriers: 68

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 22

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 640
allele frequency: 6.157398499134116e-2
allele num: 10394
num of homozygotes: 15

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

Latino
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allele count: 35
allele frequency: 3.023496890117485e-3
allele num: 11576
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 8.999010108888022e-5
allele num: 66674
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

DP
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MQ
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MQRankSum
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VQSLOD
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 3.28e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
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allele num: 10394
num of homozygotes: 0

South Asian
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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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

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

FS
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BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.406e0

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: 66602
num of homozygotes: 0

East Asian
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allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

Other
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num of homozygotes: 0

DP
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QD
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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FS
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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: 1
allele frequency: 1.503623733197005e-5
allele num: 66506
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)
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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

Other
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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
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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

QD
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SIO_000300: 1.37e1

ClippingRankSum
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SIO_000300: -5.85e-1

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

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

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

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

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

ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

African
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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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Other
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East Asian
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Latino
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MQ
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FS
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Finnish)
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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MQ
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BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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DP
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MQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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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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African
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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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num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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QD
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InbreedingCoeff
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FS
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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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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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997601918465228e-5
allele num: 66720
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
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num of homozygotes: 0

South Asian
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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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num of homozygotes: 0

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

East Asian
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allele num: 8654
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Other
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MQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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QD
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FS
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DP
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

African
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allele count: 0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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European (Non-Finnish)
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Other
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BaseQRankSum
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MQ
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MQRankSum
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FS
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VQSLOD
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ClippingRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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Latino
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InbreedingCoeff
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VQSLOD
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MQ
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FS
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DP
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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QD
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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
all individuals: 8
bin: 3.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.14151e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-1

FS
type: SiteQuality
SIO_000300: 2.344e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.787e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e0

VQSLOD
type: SiteQuality
SIO_000300: -2.626e-1

QD
type: SiteQuality
SIO_000300: 1.24e1

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3717
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2206
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2952
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3510
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2383
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2576
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8403
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 51487
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1330
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 778
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 8.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1147
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2565
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 776
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 4.141673e6

VQSLOD
type: SiteQuality
SIO_000300: 6.03e-1

QD
type: SiteQuality
SIO_000300: 9.75e0

MQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.37e-1