3-49899446-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899446
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899446
    reference: chr 3
allele count: 1
allele frequency: 8.398280032249395e-6
allele num: 119072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.387+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.227+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+319G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.227+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.227+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.2+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.409+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.227+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.245+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.245+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+319G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.227+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.506+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.227+32G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.186+73G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

3-49899451-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899451
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899451
    reference: chr 3
allele count: 14
allele frequency: 1.173846695621552e-4
allele num: 119266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.387+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.227+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.186+68G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.227+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.506+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+314G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.245+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.227+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.227+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.227+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.409+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+314G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.245+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.2+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.227+27G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18884
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9722
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14379
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

3-49899452-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899452
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899452
    reference: chr 3
allele count: 2
allele frequency: 1.677880501350694e-5
allele num: 119198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.227+26C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.186+67C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.227+26C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.2+26C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.227+26C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.245+26C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.245+26C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.506+26C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.409+26C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+313C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+313C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.227+26C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.227+26C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.227+26C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.387+26C>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-49899456-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899456
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899456
    reference: chr 3
allele count: 4
allele frequency: 3.347224314237419e-5
allele num: 119502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+309G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.387+22G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.409+22G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.245+22G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.186+63G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.227+22G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.227+22G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+309G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.2+22G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.227+22G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.227+22G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.245+22G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.227+22G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.227+22G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.506+22G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14886
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-49899467-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899467
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899467
    reference: chr 3
allele count: 1
allele frequency: 8.343902276216541e-6
allele num: 119848
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.387+11G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.245+11G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.227+11G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.2+11G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.227+11G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.245+11G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.227+11G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.227+11G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+298G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.409+11G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+298G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.186+52G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.227+11G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.227+11G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.506+11G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15615
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD

3-49899469-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899469
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899469
    reference: chr 3
allele count: 1
allele frequency: 8.338892595063375e-6
allele num: 119920
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.227+9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.186+50G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+296G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.227+9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.227+9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+296G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.245+9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.227+9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.506+9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.227+9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.245+9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.409+9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.2+9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.227+9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.387+9G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10585
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

3-49899492-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899492
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899492
    reference: chr 3
allele count: 1
allele frequency: 8.308822307526131e-6
allele num: 120354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-13A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.213A>G
  hgvsp: ENSP00000420766.1:p.Ile71Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.213A>G
  hgvsp: ENSP00000417614.1:p.Ile71Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+273A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.492A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.231A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+273A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.213A>G
  hgvsp: ENSP00000419195.1:p.Ile71Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.231A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.213A>G
  hgvsp: ENSP00000418809.1:p.Ile71Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.213A>G
  hgvsp: ENSP00000420724.1:p.Ile71Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.373A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.186+27A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.395A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.213A>G
  hgvsp: ENSP00000296471.6:p.Ile71Met
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19233
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile71Met
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

3-49899523-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899523
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899523
    reference: chr 3
allele count: 1
allele frequency: 8.292699107705576e-6
allele num: 120588
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.182G>A
  hgvsp: ENSP00000418809.1:p.Arg61His
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.182G>A
  hgvsp: ENSP00000420724.1:p.Arg61His
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+242G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.182G>A
  hgvsp: ENSP00000420139.1:p.Arg61His
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.182G>A
  hgvsp: ENSP00000417614.1:p.Arg61His
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.182G>A
  hgvsp: ENSP00000420766.1:p.Arg61His
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.182G>A
  hgvsp: ENSP00000296471.6:p.Arg61His
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.364G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-44G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.200G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.182G>A
  hgvsp: ENSP00000419195.1:p.Arg61His
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.342G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.461G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.200G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+242G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg61His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-49899525-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899525
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899525
    reference: chr 3
allele count: 2
allele frequency: 1.657824933687002e-5
allele num: 120640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.198C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.180C>A
  hgvsp: ENST00000487726.1:c.180C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.180C>A
  hgvsp: ENST00000466940.1:c.180C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.180C>A
  hgvsp: ENST00000463537.1:c.180C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.180C>A
  hgvsp: ENST00000488336.1:c.180C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+240C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-46C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.340C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.180C>A
  hgvsp: ENST00000477224.1:c.180C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.362C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.198C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.459C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+240C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.180C>A
  hgvsp: ENST00000296471.7:c.180C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.180C>A
  hgvsp: ENST00000466535.1:c.180C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly60Gly
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ

3-49899528-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899528
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899528
    reference: chr 3
allele count: 2
allele frequency: 1.657220509761029e-5
allele num: 120684
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.177C>T
  hgvsp: ENST00000296471.7:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+237C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.177C>T
  hgvsp: ENST00000477224.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.177C>T
  hgvsp: ENST00000463537.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.195C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+237C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.359C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.456C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.177C>T
  hgvsp: ENST00000466940.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.177C>T
  hgvsp: ENST00000488336.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.177C>T
  hgvsp: ENST00000487726.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.195C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-49C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.177C>T
  hgvsp: ENST00000466535.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.337C>T
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp59Asp
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

3-49899532-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899532
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899532
    reference: chr 3
allele count: 3
allele frequency: 2.485130635033715e-5
allele num: 120718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.173G>A
  hgvsp: ENSP00000420766.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.173G>A
  hgvsp: ENSP00000417614.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.173G>A
  hgvsp: ENSP00000419195.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.452G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-53G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.355G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.173G>A
  hgvsp: ENSP00000296471.6:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.173G>A
  hgvsp: ENSP00000418809.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.333G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+233G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.173G>A
  hgvsp: ENSP00000420724.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.173G>A
  hgvsp: ENSP00000420139.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+233G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.191G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.191G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg58Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

3-49899533-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899533
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899533
    reference: chr 3
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.354C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.172C>T
  hgvsp: ENSP00000420139.1:p.Arg58Trp
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.332C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.172C>T
  hgvsp: ENSP00000420766.1:p.Arg58Trp
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.172C>T
  hgvsp: ENSP00000417614.1:p.Arg58Trp
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.172C>T
  hgvsp: ENSP00000419195.1:p.Arg58Trp
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.190C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.172C>T
  hgvsp: ENSP00000296471.6:p.Arg58Trp
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-54C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.172C>T
  hgvsp: ENSP00000418809.1:p.Arg58Trp
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+232C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.172C>T
  hgvsp: ENSP00000420724.1:p.Arg58Trp
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.190C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.451C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+232C>T
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg58Trp
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

3-49899533-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899533
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899533
    reference: chr 3
allele count: 60
allele frequency: 4.969602597445624e-4
allele num: 120734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+232C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.354C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-54C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.172C>A
  hgvsp: ENST00000477224.1:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+232C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.190C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.172C>A
  hgvsp: ENST00000466940.1:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.172C>A
  hgvsp: ENST00000463537.1:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.172C>A
  hgvsp: ENST00000466535.1:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.451C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.332C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.172C>A
  hgvsp: ENST00000296471.7:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.172C>A
  hgvsp: ENST00000487726.1:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.190C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.172C>A
  hgvsp: ENST00000488336.1:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17698
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg58Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

3-49899549-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899549
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899549
    reference: chr 3
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.338C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-70C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+216C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.174C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.156C>T
  hgvsp: ENST00000477224.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.156C>T
  hgvsp: ENST00000487726.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.156C>T
  hgvsp: ENST00000466940.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.156C>T
  hgvsp: ENST00000488336.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.174C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.156C>T
  hgvsp: ENST00000466535.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.435C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.156C>T
  hgvsp: ENST00000463537.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.156C>T
  hgvsp: ENST00000296471.7:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+216C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.316C>T
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18095
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys52Cys
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-49899553-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899553
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899553
    reference: chr 3
allele count: 1
allele frequency: 8.264599414866361e-6
allele num: 120998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.152C>A
  hgvsp: ENSP00000417614.1:p.Thr51Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.152C>A
  hgvsp: ENSP00000420724.1:p.Thr51Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.312C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.152C>A
  hgvsp: ENSP00000418809.1:p.Thr51Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.170C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.152C>A
  hgvsp: ENSP00000420766.1:p.Thr51Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.431C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.152C>A
  hgvsp: ENSP00000420139.1:p.Thr51Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.170C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-74C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.152C>A
  hgvsp: ENSP00000296471.6:p.Thr51Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+212C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.334C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.152C>A
  hgvsp: ENSP00000419195.1:p.Thr51Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+212C>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17796
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr51Asn
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

3-49899559-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899559
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899559
    reference: chr 3
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.306T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+206T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.146T>C
  hgvsp: ENSP00000296471.6:p.Leu49Pro
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.328T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.146T>C
  hgvsp: ENSP00000417614.1:p.Leu49Pro
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-80T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.425T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.146T>C
  hgvsp: ENSP00000419195.1:p.Leu49Pro
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.164T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.146T>C
  hgvsp: ENSP00000418809.1:p.Leu49Pro
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.146T>C
  hgvsp: ENSP00000420724.1:p.Leu49Pro
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.146T>C
  hgvsp: ENSP00000420766.1:p.Leu49Pro
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+206T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.164T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.146T>C
  hgvsp: ENSP00000420139.1:p.Leu49Pro
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu49Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

3-49899564-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899564
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899564
    reference: chr 3
allele count: 1
allele frequency: 8.262687356435807e-6
allele num: 121026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.141C>G
  hgvsp: ENST00000488336.1:c.141C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.141C>G
  hgvsp: ENST00000466535.1:c.141C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.301C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.141C>G
  hgvsp: ENST00000487726.1:c.141C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.141C>G
  hgvsp: ENST00000466940.1:c.141C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+201C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+201C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.141C>G
  hgvsp: ENST00000296471.7:c.141C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.159C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-85C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.141C>G
  hgvsp: ENST00000477224.1:c.141C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.141C>G
  hgvsp: ENST00000463537.1:c.141C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.420C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.159C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.323C>G
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly47Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

3-49899567-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899567
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899567
    reference: chr 3
allele count: 1
allele frequency: 8.261322141995606e-6
allele num: 121046
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.138A>G
  hgvsp: ENST00000466535.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.138A>G
  hgvsp: ENST00000466940.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.320A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.138A>G
  hgvsp: ENST00000488336.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-88A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.298A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.138A>G
  hgvsp: ENST00000487726.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.156A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.138A>G
  hgvsp: ENST00000477224.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.138A>G
  hgvsp: ENST00000296471.7:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.138A>G
  hgvsp: ENST00000463537.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.156A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+198A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+198A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.417A>G
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr46Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

3-49899570-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899570
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899570
    reference: chr 3
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.153G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+195G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.135G>A
  hgvsp: ENST00000488336.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.135G>A
  hgvsp: ENST00000466535.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.135G>A
  hgvsp: ENST00000487726.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.153G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.135G>A
  hgvsp: ENST00000296471.7:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.135G>A
  hgvsp: ENST00000463537.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-91G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+195G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.414G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.135G>A
  hgvsp: ENST00000466940.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.135G>A
  hgvsp: ENST00000477224.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.317G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.295G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17459
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr45Thr
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

3-49899571-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899571
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899571
    reference: chr 3
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+194C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.134C>T
  hgvsp: ENSP00000420139.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.152C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.134C>T
  hgvsp: ENSP00000418809.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.134C>T
  hgvsp: ENSP00000420724.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.134C>T
  hgvsp: ENSP00000417614.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.134C>T
  hgvsp: ENSP00000419195.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.134C>T
  hgvsp: ENSP00000420766.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-92C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.413C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.316C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+194C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.152C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.134C>T
  hgvsp: ENSP00000296471.6:p.Thr45Met
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.294C>T
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr45Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

3-49899579-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899579
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899579
    reference: chr 3
allele count: 1
allele frequency: 8.257501940512956e-6
allele num: 121102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.144G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.286G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-100G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.126G>A
  hgvsp: ENST00000466940.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.126G>A
  hgvsp: ENST00000296471.7:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+186G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.126G>A
  hgvsp: ENST00000488336.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.126G>A
  hgvsp: ENST00000466535.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.126G>A
  hgvsp: ENST00000487726.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.126G>A
  hgvsp: ENST00000463537.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+186G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.126G>A
  hgvsp: ENST00000477224.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.144G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.308G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.405G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys42Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

3-49899591-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899591
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899591
    reference: chr 3
allele count: 67
allele frequency: 5.53079082053822e-4
allele num: 121140
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.114C>A
  hgvsp: ENST00000477224.1:c.114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.114C>A
  hgvsp: ENST00000488336.1:c.114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-112C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.296C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+174C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.393C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.114C>A
  hgvsp: ENST00000296471.7:c.114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.114C>A
  hgvsp: ENST00000466535.1:c.114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.114C>A
  hgvsp: ENST00000463537.1:c.114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+174C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.114C>A
  hgvsp: ENST00000487726.1:c.114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.132C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.114C>A
  hgvsp: ENST00000466940.1:c.114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.274C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.132C>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12787
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Ile38Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

3-49899600-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899600
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899600
    reference: chr 3
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.123T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.105T>C
  hgvsp: ENST00000466535.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.105T>C
  hgvsp: ENST00000466940.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.105T>C
  hgvsp: ENST00000477224.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-121T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.105T>C
  hgvsp: ENST00000487726.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.105T>C
  hgvsp: ENST00000488336.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.105T>C
  hgvsp: ENST00000463537.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.123T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+165T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.384T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+165T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.105T>C
  hgvsp: ENST00000296471.7:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.265T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.287T>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe35Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-49899617-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899617
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899617
    reference: chr 3
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.96-8G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.96-8G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.278-8G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.114-8G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.96-8G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.114-8G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+148G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.96-8G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-130-8G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.367G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.256-8G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.96-8G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.96-8G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+148G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.96-8G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.96-8G>C
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

3-49899617-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899617
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899617
    reference: chr 3
allele count: 5
allele frequency: 4.127183279955096e-5
allele num: 121148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.96-8G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.278-8G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.96-8G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+148G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.114-8G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.114-8G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.96-8G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+148G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.256-8G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.367G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.96-8G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.96-8G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.96-8G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.96-8G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-130-8G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16611
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.96-8G>A
num of homozygotes: 1
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

3-49899618-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899618
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899618
    reference: chr 3
allele count: 1
allele frequency: 8.255047961828658e-6
allele num: 121138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.278-9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.114-9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.114-9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+147C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.366C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.96-9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.96-9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.96-9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.96-9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.256-9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+147C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-130-9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.96-9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.96-9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.96-9C>T
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-49899630-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899630
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899630
    reference: chr 3
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.278-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.96-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-130-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.96-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.96-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.354G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.114-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.96-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.96-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+135G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.96-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.114-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.96-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.256-21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+135G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

3-49899640-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899640
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899640
    reference: chr 3
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+125C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.96-31C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.114-31C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.96-31C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-130-31C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.278-31C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+125C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.96-31C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.114-31C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.96-31C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.96-31C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.96-31C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.256-31C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.344C>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.96-31C>A
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

3-49899651-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899651
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899651
    reference: chr 3
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.96-42T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.96-42T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.114-42T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.96-42T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.256-42T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.114-42T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.333T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-130-42T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.278-42T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+114T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+114T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.96-42T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.96-42T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.96-42T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.96-42T>C
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

3-49899657-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899657
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899657
    reference: chr 3
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.96-48T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.96-48T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.114-48T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-130-48T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.114-48T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.278-48T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.327T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+108T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.256-48T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.96-48T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.96-48T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+108T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.96-48T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.96-48T>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.96-48T>A
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

3-49899658-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899658
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899658
    reference: chr 3
allele count: 2
allele frequency: 1.650491846570278e-5
allele num: 121176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.256-49G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.114-49G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+107G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.96-49G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.96-49G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.96-49G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.96-49G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+107G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.277+49G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-130-49G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.96-49G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.96-49G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.114-49G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.326G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.96-49G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

3-49899680-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899680
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899680
    reference: chr 3
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.277+27G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-130-71G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.95+47G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.113+47G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.95+47G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+85G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.304G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.255+47G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.95+47G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.113+47G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+85G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.95+47G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.95+47G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.95+47G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.95+47G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

3-49899684-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899684
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899684
    reference: chr 3
allele count: 5
allele frequency: 4.12044896411913e-5
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.95+43G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.95+43G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.277+23G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.95+43G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.300G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.113+43G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.255+43G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.95+43G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.113+43G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-130-75G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+81G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+81G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.95+43G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.95+43G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.95+43G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6048
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

3-49899709-GAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899709
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899707
    reference: chr 3
allele count: 4
allele frequency: 3.29549012176836e-5
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.255+16_255+17delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+54_57+55delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.273_274delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.113+16_113+17delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.113+16_113+17delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.273_274delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+54_219+55delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.95+16_95+17delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.95+16_95+17delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.95+16_95+17delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.95+16_95+17delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.95+16_95+17delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131+54_-131+55delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.95+16_95+17delGT
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.95+16_95+17delGT
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: GAC
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

3-49899712-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899712
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899712
    reference: chr 3
allele count: 4
allele frequency: 3.295381522795802e-5
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.95+15T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131+53T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+53T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+53T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.95+15T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.95+15T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.95+15T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.95+15T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.272T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.95+15T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.255+15T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.113+15T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.113+15T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.272T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.95+15T>C
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum

3-49899717-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899717
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899717
    reference: chr 3
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.95+10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.267G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131+48G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.267G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.95+10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.113+10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+48G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.113+10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.95+10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+48G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.95+10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.255+10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.95+10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.95+10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.95+10G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

3-49899717-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899717
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899717
    reference: chr 3
allele count: 9
allele frequency: 7.41485277397881e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+48G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.267G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131+48G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.255+10G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.95+10G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.95+10G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.95+10G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.267G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.113+10G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.95+10G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.95+10G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.113+10G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.95+10G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+48G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.95+10G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

3-49899718-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899718
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899718
    reference: chr 3
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.95+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.113+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.95+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.95+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.95+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.95+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.266C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+47C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.113+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.266C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131+47C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.255+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.95+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+47C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.95+9C>T
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-49899718-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899718
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899718
    reference: chr 3
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.266C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131+47C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.95+9C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.113+9C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.95+9C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.255+9C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.266C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+47C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.95+9C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.95+9C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+47C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.95+9C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.113+9C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.95+9C>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.95+9C>G
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

3-49899720-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899720
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899720
    reference: chr 3
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.95+7G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.264G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.95+7G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.113+7G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.255+7G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.95+7G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.95+7G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.95+7G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.95+7G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+45G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.95+7G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.264G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131+45G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.113+7G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+45G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.95+7G>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

3-49899735-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899735
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899735
    reference: chr 3
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.249C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.87C>T
  hgvsp: ENST00000466535.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.87C>T
  hgvsp: ENST00000487726.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.87C>T
  hgvsp: ENST00000477224.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+30C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.87C>T
  hgvsp: ENST00000488336.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+30C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.105C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.105C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131+30C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.87C>T
  hgvsp: ENST00000296471.7:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.87C>T
  hgvsp: ENST00000466940.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.249C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.247C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.87C>T
  hgvsp: ENST00000463537.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val29Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-49899744-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899744
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899744
    reference: chr 3
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.78G>A
  hgvsp: ENST00000466535.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.240G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.78G>A
  hgvsp: ENST00000487726.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.78G>A
  hgvsp: ENST00000477224.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.96G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.96G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.78G>A
  hgvsp: ENST00000466940.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131+21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.78G>A
  hgvsp: ENST00000463537.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.238G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.78G>A
  hgvsp: ENST00000296471.7:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.240G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+21G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.78G>A
  hgvsp: ENST00000488336.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu26Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ

3-49899747-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899747
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899747
    reference: chr 3
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.75T>C
  hgvsp: ENST00000296471.7:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.235T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.75T>C
  hgvsp: ENST00000463537.1:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.75T>C
  hgvsp: ENST00000477224.1:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.75T>C
  hgvsp: ENST00000487726.1:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.75T>C
  hgvsp: ENST00000466535.1:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131+18T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+18T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.75T>C
  hgvsp: ENST00000466940.1:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.93T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+18T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.93T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.75T>C
  hgvsp: ENST00000488336.1:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.237T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.237T>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp25Asp
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

3-49899756-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899756
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899756
    reference: chr 3
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.66C>T
  hgvsp: ENST00000477224.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.66C>T
  hgvsp: ENST00000488336.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.66C>T
  hgvsp: ENST00000466535.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.84C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.66C>T
  hgvsp: ENST00000487726.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.66C>T
  hgvsp: ENST00000466940.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.226C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.228C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.66C>T
  hgvsp: ENST00000463537.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131+9C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.228C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.84C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.66C>T
  hgvsp: ENST00000296471.7:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp22Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

3-49899765-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899765
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899765
    reference: chr 3
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.57G>A
  hgvsp: ENST00000463537.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.57G>A
  hgvsp: ENST00000487726.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.57G>A
  hgvsp: ENST00000296471.7:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.217G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.75G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.219G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-131G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.57G>A
  hgvsp: ENST00000466940.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.57G>A
  hgvsp: ENST00000480398.2:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.57G>A
  hgvsp: ENST00000466535.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.219G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.57G>A
  hgvsp: ENST00000477224.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.75G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.57G>A
  hgvsp: ENST00000488336.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.219G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-131G>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/3-49899768-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899768
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899768
    reference: chr 3
allele count: 5
allele frequency: 4.118819711023609e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.216G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.54G>T
  hgvsp: ENST00000466535.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.54G>T
  hgvsp: ENST00000296471.7:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.54G>T
  hgvsp: ENST00000487726.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-134G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.54G>T
  hgvsp: ENST00000488336.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.54G>T
  hgvsp: ENST00000463537.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.216G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.54G>T
  hgvsp: ENST00000477224.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.54G>T
  hgvsp: ENST00000466940.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.54G>T
  hgvsp: ENST00000480398.2:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.72G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.72G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.216G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.214G>T
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser18Ser
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

3-49899768-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899768
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899768
    reference: chr 3
allele count: 7
allele frequency: 5.766347595433053e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.54G>A
  hgvsp: ENST00000466535.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.54G>A
  hgvsp: ENST00000480398.2:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.72G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.54G>A
  hgvsp: ENST00000487726.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.54G>A
  hgvsp: ENST00000488336.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.216G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.54G>A
  hgvsp: ENST00000296471.7:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-134G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.54G>A
  hgvsp: ENST00000463537.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.216G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.214G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.54G>A
  hgvsp: ENST00000466940.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.54G>A
  hgvsp: ENST00000477224.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.216G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.72G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser18Ser
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

3-49899786-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899786
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899786
    reference: chr 3
allele count: 4
allele frequency: 3.295272930980509e-5
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.36G>C
  hgvsp: ENSP00000418809.1:p.Lys12Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.36G>C
  hgvsp: ENSP00000417614.1:p.Lys12Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.198G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.36G>C
  hgvsp: ENSP00000420139.1:p.Lys12Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-152G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.36G>C
  hgvsp: ENSP00000420766.1:p.Lys12Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.36G>C
  hgvsp: ENSP00000420000.2:p.Lys12Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.36G>C
  hgvsp: ENSP00000296471.6:p.Lys12Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.36G>C
  hgvsp: ENSP00000419195.1:p.Lys12Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.198G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.54G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.198G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.54G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.36G>C
  hgvsp: ENSP00000420724.1:p.Lys12Asn
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.196G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys12Asn
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP

3-49899786-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899786
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899786
    reference: chr 3
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.198G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.198G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.36G>A
  hgvsp: ENST00000488336.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.54G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.36G>A
  hgvsp: ENST00000487726.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.36G>A
  hgvsp: ENST00000477224.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.36G>A
  hgvsp: ENST00000463537.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.36G>A
  hgvsp: ENST00000296471.7:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.196G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-152G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.36G>A
  hgvsp: ENST00000480398.2:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.36G>A
  hgvsp: ENST00000466535.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.36G>A
  hgvsp: ENST00000466940.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.54G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.198G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys12Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

3-49899792-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899792
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899792
    reference: chr 3
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.190C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.48C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.30C>T
  hgvsp: ENST00000488336.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.30C>T
  hgvsp: ENST00000463537.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.192C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.30C>T
  hgvsp: ENST00000466940.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.30C>T
  hgvsp: ENST00000466535.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.48C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-158C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.192C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.30C>T
  hgvsp: ENST00000487726.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.30C>T
  hgvsp: ENST00000480398.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.192C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.30C>T
  hgvsp: ENST00000296471.7:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.30C>T
  hgvsp: ENST00000477224.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp10Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

3-49899795-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899795
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899795
    reference: chr 3
allele count: 39573
allele frequency: 3.260955551526938e-1
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.27C>T
  hgvsp: ENST00000466940.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.27C>T
  hgvsp: ENST00000487726.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.187C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.27C>T
  hgvsp: ENST00000480398.2:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.27C>T
  hgvsp: ENST00000296471.7:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.27C>T
  hgvsp: ENST00000488336.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.189C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.45C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.27C>T
  hgvsp: ENST00000463537.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-161C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.27C>T
  hgvsp: ENST00000477224.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.45C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.189C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.27C>T
  hgvsp: ENST00000466535.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.189C>T
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 9.25e1
  variant carriers: 1979
genotype depth: GenotypeDepth
  all individuals: 6214
  bin: 2.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 3.25e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.75e1
  variant carriers: 237
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 8.75e1
  variant carriers: 1898
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.75e1
  variant carriers: 920
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 1206
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Gly9Gly
num of homozygotes: 7202
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

3-49899800-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899800
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899800
    reference: chr 3
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.22C>T
  hgvsp: ENST00000466535.1:c.22C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-166C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.22C>T
  hgvsp: ENST00000487726.1:c.22C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.22C>T
  hgvsp: ENST00000466940.1:c.22C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.22C>T
  hgvsp: ENST00000477224.1:c.22C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.182C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.22C>T
  hgvsp: ENST00000480398.2:c.22C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.184C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.40C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.40C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.22C>T
  hgvsp: ENST00000463537.1:c.22C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.184C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.184C>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.22C>T
  hgvsp: ENST00000488336.1:c.22C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.22C>T
  hgvsp: ENST00000296471.7:c.22C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14228
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu8Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

3-49899804-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899804
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899804
    reference: chr 3
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.180G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.18G>C
  hgvsp: ENST00000466535.1:c.18G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.18G>C
  hgvsp: ENST00000477224.1:c.18G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.18G>C
  hgvsp: ENST00000296471.7:c.18G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.18G>C
  hgvsp: ENST00000463537.1:c.18G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.18G>C
  hgvsp: ENST00000487726.1:c.18G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.180G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-170G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.36G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.18G>C
  hgvsp: ENST00000488336.1:c.18G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.18G>C
  hgvsp: ENST00000480398.2:c.18G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.18G>C
  hgvsp: ENST00000466940.1:c.18G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.178G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.36G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.180G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val6Val
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

3-49899831-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899831
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899831
    reference: chr 3
allele count: 5
allele frequency: 4.122487343963854e-5
allele num: 121286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.153G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.153G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-197G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.151G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.9G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.153G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/3-49899835-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899835
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899835
    reference: chr 3
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.-14G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.-14G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.5G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.-14G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.149G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.149G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.147G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-201G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.-14G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.-14G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.-14G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.149G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.-14G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.-14G>T
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.5G>T
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14068
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-14G>T
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

3-49899839-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899839
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899839
    reference: chr 3
allele count: 28
allele frequency: 2.309125995810586e-4
allele num: 121258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.149-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.-14-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.-14-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.-14-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.147-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.149-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.149-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.-14-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.-14-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000483811
  gene symbol: CAMKV
  hgvsc: ENST00000483811.1:n.1G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.-14-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.-14-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.-14-4G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000472895
  gene symbol: CAMKV
  hgvsc: ENST00000472895.1:n.1G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-201-4G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10113
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.-14-4G>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

3-49899845-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899845
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899845
    reference: chr 3
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.-14-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.149-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.-14-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.147-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.-14-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.-14-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.149-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.149-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-201-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.-14-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.-14-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.-14-10G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.-14-10G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

3-49899868-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899868
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899868
    reference: chr 3
allele count: 1359
allele frequency: 1.12453454695904e-2
allele num: 120850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.149-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.-14-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.-14-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.-14-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.149-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.-14-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.149-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.-14-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.147-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-201-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.-14-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.-14-33G>A
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.-14-33G>A
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6879
  bin: 2.25e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 5.25e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 11462
  bin: 3.25e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 10630
  bin: 2.75e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9150
  bin: 3.75e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 1.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 4.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 4.25e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
num of homozygotes: 75
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

3-49899870-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899870
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899870
    reference: chr 3
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.-14-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.-14-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.-14-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.149-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.-14-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.-14-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.147-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.-14-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.-14-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.149-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-201-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.149-35T>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.-14-35T>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10705
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3646
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6280
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS

3-49899872-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899872
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899872
    reference: chr 3
allele count: 53
allele frequency: 4.387780445401109e-4
allele num: 120790
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.-14-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.147-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-201-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.149-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.-14-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.-14-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.-14-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.-14-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.-14-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.149-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.149-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.-14-37A>G
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.-14-37A>G
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9066
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 10738
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

3-49899873-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49899873
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49899873
    reference: chr 3
allele count: 4
allele frequency: 3.31273913835655e-5
allele num: 120746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000417614
  ensembl transcript: ENST00000463537
  gene symbol: CAMKV
  hgvsc: ENST00000463537.1:c.-14-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000475665
  gene symbol: CAMKV
  hgvsc: ENST00000475665.1:n.147-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000498324
  gene symbol: CAMKV
  hgvsc: ENST00000498324.1:n.149-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000479704
  gene symbol: CAMKV
  hgvsc: ENST00000479704.1:n.149-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420139
  ensembl transcript: ENST00000487726
  gene symbol: CAMKV
  hgvsc: ENST00000487726.1:c.-14-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000296471
  ensembl transcript: ENST00000296471
  gene symbol: CAMKV
  hgvsc: ENST00000296471.7:c.-14-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420724
  ensembl transcript: ENST00000466940
  gene symbol: CAMKV
  hgvsc: ENST00000466940.1:c.-14-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl transcript: ENST00000476105
  gene symbol: CAMKV
  hgvsc: ENST00000476105.1:n.149-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000418809
  ensembl transcript: ENST00000488336
  gene symbol: CAMKV
  hgvsc: ENST00000488336.1:c.-14-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420000
  ensembl transcript: ENST00000480398
  gene symbol: CAMKV
  hgvsc: ENST00000480398.2:c.-14-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000419195
  ensembl transcript: ENST00000477224
  gene symbol: CAMKV
  hgvsc: ENST00000477224.1:c.-14-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420766
  ensembl transcript: ENST00000466535
  gene symbol: CAMKV
  hgvsc: ENST00000466535.1:c.-14-38G>C
  variant of: http://identifiers.org/hgnc/28788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164076
  ensembl protein: ENSP00000420053
  ensembl transcript: ENST00000467248
  gene symbol: CAMKV
  hgvsc: ENST00000467248.1:c.-201-38G>C
  variant of: http://identifiers.org/hgnc/28788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10946
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9051
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

3-49924694-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49924694
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49924694
    reference: chr 3
allele count: 1
allele frequency: 8.523986498005388e-6
allele num: 117316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000407926
  ensembl transcript: ENST00000411578
  gene symbol: MST1R
  hgvsc: ENST00000411578.2:c.*1071A>G
  variant of: http://identifiers.org/hgnc/7381
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000341325
  ensembl transcript: ENST00000344206
  gene symbol: MST1R
  hgvsc: ENST00000344206.4:c.*46A>G
  variant of: http://identifiers.org/hgnc/7381
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000296474
  ensembl transcript: ENST00000296474
  gene symbol: MST1R
  hgvsc: ENST00000296474.3:c.*46A>G
  variant of: http://identifiers.org/hgnc/7381
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45182
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-49924695-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49924695
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49924695
    reference: chr 3
allele count: 2
allele frequency: 1.704535769683127e-5
allele num: 117334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000341325
  ensembl transcript: ENST00000344206
  gene symbol: MST1R
  hgvsc: ENST00000344206.4:c.*45C>G
  variant of: http://identifiers.org/hgnc/7381
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000407926
  ensembl transcript: ENST00000411578
  gene symbol: MST1R
  hgvsc: ENST00000411578.2:c.*1070C>G
  variant of: http://identifiers.org/hgnc/7381
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000296474
  ensembl transcript: ENST00000296474
  gene symbol: MST1R
  hgvsc: ENST00000296474.3:c.*45C>G
  variant of: http://identifiers.org/hgnc/7381
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1919
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45182
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2389
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

3-49924696-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49924696
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49924696
    reference: chr 3
allele count: 1
allele frequency: 8.520209937972871e-6
allele num: 117368
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000296474
  ensembl transcript: ENST00000296474
  gene symbol: MST1R
  hgvsc: ENST00000296474.3:c.*44C>G
  variant of: http://identifiers.org/hgnc/7381
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000341325
  ensembl transcript: ENST00000344206
  gene symbol: MST1R
  hgvsc: ENST00000344206.4:c.*44C>G
  variant of: http://identifiers.org/hgnc/7381
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000407926
  ensembl transcript: ENST00000411578
  gene symbol: MST1R
  hgvsc: ENST00000411578.2:c.*1069C>G
  variant of: http://identifiers.org/hgnc/7381
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2489
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1959
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45182
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

3-49924697-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49924697
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 49924697
    reference: chr 3
allele count: 1
allele frequency: 8.518903446748335e-6
allele num: 117386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000341325
  ensembl transcript: ENST00000344206
  gene symbol: MST1R
  hgvsc: ENST00000344206.4:c.*43C>T
  variant of: http://identifiers.org/hgnc/7381
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000407926
  ensembl transcript: ENST00000411578
  gene symbol: MST1R
  hgvsc: ENST00000411578.2:c.*1068C>T
  variant of: http://identifiers.org/hgnc/7381
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164078
  ensembl protein: ENSP00000296474
  ensembl transcript: ENST00000296474
  gene symbol: MST1R
  hgvsc: ENST00000296474.3:c.*43C>T
  variant of: http://identifiers.org/hgnc/7381
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45180
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: G

GenotypeDepth
all individuals: 13576
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9193
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4015
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2053
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7047
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1538
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19498
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2085
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4354
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3908
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1367
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7620
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1665
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.165228113440197e-5
allele num: 16220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.8e-1

DP
type: SiteQuality
SIO_000300: 1.71721e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.752e0

QD
type: SiteQuality
SIO_000300: 9.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-1

GenotypeDepth
all individuals: 891
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 932
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 285
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variant carriers: 0

GenotypeDepth
all individuals: 1996
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variant carriers: 1

GenotypeDepth
all individuals: 183
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variant carriers: 0

GenotypeDepth
all individuals: 4247
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variant carriers: 1

GenotypeQuality
all individuals: 8027
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 4547
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variant carriers: 0

GenotypeQuality
all individuals: 834
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variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 494
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variant carriers: 0

GenotypeQuality
all individuals: 1673
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variant carriers: 0

GenotypeQuality
all individuals: 7108
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variant carriers: 14

GenotypeQuality
all individuals: 1749
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variant carriers: 0

GenotypeQuality
all individuals: 73
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variant carriers: 0

GenotypeQuality
all individuals: 3339
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variant carriers: 0

GenotypeQuality
all individuals: 650
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variant carriers: 0

GenotypeQuality
all individuals: 1087
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variant carriers: 0

GenotypeQuality
all individuals: 736
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variant carriers: 0

GenotypeQuality
all individuals: 21199
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4145
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 1

GenotypeQuality
all individuals: 1565
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1613
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.978239366963402e-4
allele num: 10110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523229246001523e-5
allele num: 65650
num of homozygotes: 0

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

South Asian
type: Population
allele count: 11
allele frequency: 6.777572396796057e-4
allele num: 16230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

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

Other
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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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allele frequency: 0.0e0
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East Asian
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South Asian
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African
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InbreedingCoeff
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ClippingRankSum
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QD
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MQ
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FS
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DP
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MQRankSum
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VQSLOD
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BaseQRankSum
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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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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

Latino
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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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele num: 8600
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South Asian
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Other
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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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DP
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VQSLOD
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MQRankSum
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ReadPosRankSum
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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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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 65920
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Other
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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African
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ReadPosRankSum
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SIO_000300: -3.44e-1

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

European (Non-Finnish)
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East Asian
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Other
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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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VQSLOD
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FS
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QD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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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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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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num of homozygotes: 0

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

African
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.013954609843576e-5
allele num: 66358
num of homozygotes: 0

South Asian
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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

Other
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
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BaseQRankSum
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SIO_000300: -2.151e0

VQSLOD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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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: 2
allele frequency: 3.012864933265042e-5
allele num: 66382
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
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SIO_000300: 1.838315e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: 1.7e-2

BaseQRankSum
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SIO_000300: -4.51e-1

MQ
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SIO_000300: 5.829e1

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.517800132522137e-5
allele num: 66404
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African
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East Asian
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InbreedingCoeff
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QD
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FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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MQRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11508
num of homozygotes: 0

Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 25
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allele num: 66420
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East Asian
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Other
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African
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Latino
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South Asian
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European (Finnish)
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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QD
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FS
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MQRankSum
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DP
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VQSLOD
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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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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: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

Other
type: Population
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Latino
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allele count: 0
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European (Non-Finnish)
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allele count: 0
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African
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European (Finnish)
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East Asian
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DP
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MQRankSum
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QD
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SIO_000300: 1.282e1

MQ
type: SiteQuality
SIO_000300: 5.859e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.067e0

ClippingRankSum
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SIO_000300: -8.88e-1

VQSLOD
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SIO_000300: -1.776e0

BaseQRankSum
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SIO_000300: -1.379e0

ReadPosRankSum
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SIO_000300: 1.4e0

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 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
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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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.858566e6

VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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QD
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FS
type: SiteQuality
SIO_000300: 4.927e0

BaseQRankSum
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SIO_000300: 3.39e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502855425308085e-5
allele num: 66540
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6544
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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

ReadPosRankSum
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SIO_000300: -1.49e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 4.186e0

MQRankSum
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SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: 5.3e-1

DP
type: SiteQuality
SIO_000300: 1.860872e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.49e-1

QD
type: SiteQuality
SIO_000300: 1.224e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeDepth
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variant carriers: 0

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

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

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

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

South Asian
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allele num: 16484
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 (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
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SIO_000300: 1.863092e6

MQ
type: SiteQuality
SIO_000300: 5.871e1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.75e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6546
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

South Asian
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allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

East Asian
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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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MQRankSum
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SIO_000300: 1.45e-1

BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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FS
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MQ
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DP
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InbreedingCoeff
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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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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 frequency: 0.0e0
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num of homozygotes: 0

Other
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South Asian
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African
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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allele count: 1
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allele num: 66572
num of homozygotes: 0

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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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQ
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DP
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502042778178322e-5
allele num: 66576
num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
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SIO_000300: -2.291e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

QD
type: SiteQuality
SIO_000300: 1.4e1

FS
type: SiteQuality
SIO_000300: 1.7503e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 1.867078e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
all individuals: 23587
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7354
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4163
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 3.074e0

VQSLOD
type: SiteQuality
SIO_000300: -1.28e0

DP
type: SiteQuality
SIO_000300: 1.868975e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.406e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 2.398e1

GenotypeDepth
all individuals: 513
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 996
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variant carriers: 5

GenotypeDepth
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variant carriers: 7

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 112
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1967
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7423
bin: 9.75e1
variant carriers: 67

GenotypeQuality
all individuals: 1943
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

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

African
type: Population
allele count: 58
allele frequency: 5.585516178736517e-3
allele num: 10384
num of homozygotes: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.333506673600277e-4
allele num: 11538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002732486562772e-5
allele num: 66606
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212121212121212e-4
allele num: 16500
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.229e1

MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.25e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

DP
type: SiteQuality
SIO_000300: 1.873217e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

GenotypeDepth
all individuals: 290
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18582
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 1001
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 567
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GenotypeDepth
all individuals: 225
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variant carriers: 0

GenotypeDepth
all individuals: 4897
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variant carriers: 0

GenotypeDepth
all individuals: 17006
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variant carriers: 0

GenotypeQuality
all individuals: 4186
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 128
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variant carriers: 0

GenotypeQuality
all individuals: 274
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GenotypeQuality
all individuals: 9884
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variant carriers: 0

GenotypeQuality
all individuals: 116
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1970
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variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 5752
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GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 109
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variant carriers: 0

GenotypeQuality
all individuals: 7398
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variant carriers: 1

GenotypeQuality
all individuals: 1951
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
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: 904
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.580000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.449e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.88e-1

DP
type: SiteQuality
SIO_000300: 1.873402e6

QD
type: SiteQuality
SIO_000300: 1.702e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeDepth
all individuals: 358
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 314
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variant carriers: 0

GenotypeDepth
all individuals: 340
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variant carriers: 0

GenotypeDepth
all individuals: 6
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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
all individuals: 1977
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
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variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 8.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.65e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.163999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.877101e6

QD
type: SiteQuality
SIO_000300: 2.065e1

MQRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

FS
type: SiteQuality
SIO_000300: 2.216e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeDepth
all individuals: 12983
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variant carriers: 0

GenotypeDepth
all individuals: 358
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1013
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 303
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GenotypeDepth
all individuals: 18531
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variant carriers: 0

GenotypeDepth
all individuals: 314
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variant carriers: 0

GenotypeDepth
all individuals: 423
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GenotypeDepth
all individuals: 184
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GenotypeDepth
all individuals: 510
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variant carriers: 1

GenotypeDepth
all individuals: 241
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GenotypeDepth
all individuals: 284
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GenotypeQuality
all individuals: 9884
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 293
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7414
bin: 9.75e1
variant carriers: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817961459217065e-4
allele num: 16502
num of homozygotes: 1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

FS
type: SiteQuality
SIO_000300: 2.216e0

MQRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.877101e6

QD
type: SiteQuality
SIO_000300: 2.065e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.163999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.65e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 574
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 170
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.75e1
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GenotypeQuality
all individuals: 165
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GenotypeQuality
all individuals: 165
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
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variant carriers: 0

GenotypeQuality
all individuals: 5331
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4241
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501862309263487e-5
allele num: 66584
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.301e1

DP
type: SiteQuality
SIO_000300: 1.878071e6

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 1.626e0

VQSLOD
type: SiteQuality
SIO_000300: 9.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.71e-1

GenotypeDepth
all individuals: 13163
bin: 3.25e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2009
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variant carriers: 0

GenotypeQuality
all individuals: 5391
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.289e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.116e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.91e-1

FS
type: SiteQuality
SIO_000300: 1.423e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

DP
type: SiteQuality
SIO_000300: 1.882837e6

VQSLOD
type: SiteQuality
SIO_000300: 4.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e0

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7469
bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.887218e6

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.761e0

FS
type: SiteQuality
SIO_000300: 2.843e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.66e0

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.296e0

QD
type: SiteQuality
SIO_000300: 1.258e1

GenotypeDepth
all individuals: 265
bin: 1.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.892932e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
SIO_000300: -1.367e0

FS
type: SiteQuality
SIO_000300: 4.222e0

VQSLOD
type: SiteQuality
SIO_000300: 2.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.129e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

QD
type: SiteQuality
SIO_000300: 1.253e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.294e0

GenotypeDepth
all individuals: 303
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
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: 6.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.92e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.63e-1

DP
type: SiteQuality
SIO_000300: 1.898033e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

QD
type: SiteQuality
SIO_000300: 1.183e1

GenotypeDepth
all individuals: 286
bin: 7.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.086e0

QD
type: SiteQuality
SIO_000300: 1.444e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

DP
type: SiteQuality
SIO_000300: 1.899152e6

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

BaseQRankSum
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SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-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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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.379e1

BaseQRankSum
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SIO_000300: 3.02e0

FS
type: SiteQuality
SIO_000300: 4.173e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 7.495802350683618e-5
allele num: 66704
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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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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European (Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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MQ
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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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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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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

South Asian
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num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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African
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FS
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SIO_000300: 0.0e0

MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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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: 66724
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
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DP
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BaseQRankSum
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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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num of homozygotes: 0

Other
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African
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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MQRankSum
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QD
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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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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East Asian
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allele num: 8654
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Other
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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FS
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QD
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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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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African
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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European (Finnish)
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QD
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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FS
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BaseQRankSum
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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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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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ClippingRankSum
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DP
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BaseQRankSum
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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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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East Asian
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European (Finnish)
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BaseQRankSum
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FS
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DP
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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FS
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QD
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DP
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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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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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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European (Finnish)
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East Asian
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Latino
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Other
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South Asian
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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FS
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DP
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MQ
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GenotypeDepth
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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DP
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QD
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FS
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MQ
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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East Asian
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African
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MQ
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MQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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African
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Other
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European (Finnish)
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European (Non-Finnish)
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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DP
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ClippingRankSum
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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QD
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BaseQRankSum
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DP
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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Latino
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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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MQ
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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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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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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East Asian
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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MQ
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FS
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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Other
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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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DP
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ReadPosRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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East Asian
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European (Non-Finnish)
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FS
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MQRankSum
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MQ
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QD
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ReadPosRankSum
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InbreedingCoeff
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 20113

GenotypeQuality
all individuals: 2
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variant carriers: 1

GenotypeQuality
all individuals: 8
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variant carriers: 4

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 32239

GenotypeQuality
all individuals: 7245
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variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 20

GenotypeQuality
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variant carriers: 5

GenotypeQuality
all individuals: 21
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variant carriers: 7

GenotypeQuality
all individuals: 1704
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variant carriers: 9

GenotypeQuality
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bin: 2.25e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 14

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 1158
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variant carriers: 14

GenotypeQuality
all individuals: 2289
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variant carriers: 22

GenotypeQuality
all individuals: 2616
bin: 7.75e1
variant carriers: 20

East Asian
type: Population
allele count: 1049
allele frequency: 1.212997224791859e-1
allele num: 8648
num of homozygotes: 67

European (Finnish)
type: Population
allele count: 2113
allele frequency: 3.197639225181598e-1
allele num: 6608
num of homozygotes: 343

European (Non-Finnish)
type: Population
allele count: 27042
allele frequency: 4.053665117673512e-1
allele num: 66710
num of homozygotes: 5503

South Asian
type: Population
allele count: 2785
allele frequency: 1.686652131782946e-1
allele num: 16512
num of homozygotes: 230

Latino
type: Population
allele count: 2525
allele frequency: 2.182368193604149e-1
allele num: 11570
num of homozygotes: 308

African
type: Population
allele count: 3746
allele frequency: 3.602615887670706e-1
allele num: 10398
num of homozygotes: 701

Other
type: Population
allele count: 313
allele frequency: 3.447136563876652e-1
allele num: 908
num of homozygotes: 50

ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.844e0

DP
type: SiteQuality
SIO_000300: 4.576301e6

QD
type: SiteQuality
SIO_000300: 1.638e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.19e-2

MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.8e0

GenotypeDepth
all individuals: 2607
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 97
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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
all individuals: 1022
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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: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2351
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16853
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997781641585227e-5
allele num: 66716
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-1

DP
type: SiteQuality
SIO_000300: 2.245346e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.773e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.722e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.71e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 14963
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variant carriers: 1

GenotypeQuality
all individuals: 2350
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.245142e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.355e0

VQSLOD
type: SiteQuality
SIO_000300: 1.45e-1

FS
type: SiteQuality
SIO_000300: 4.817e0

QD
type: SiteQuality
SIO_000300: 1.087e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.96e-1

GenotypeDepth
all individuals: 236
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4238
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variant carriers: 0

GenotypeDepth
all individuals: 1678
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variant carriers: 1

GenotypeDepth
all individuals: 642
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 412
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GenotypeQuality
all individuals: 16712
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GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 3600
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 8787
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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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 3.850596842510589e-4
allele num: 10388
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.784e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
SIO_000300: 1.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 3.485e0

QD
type: SiteQuality
SIO_000300: 2.922e1

DP
type: SiteQuality
SIO_000300: 2.239633e6

GenotypeDepth
all individuals: 15695
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
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variant carriers: 0

GenotypeDepth
all individuals: 319
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GenotypeDepth
all individuals: 1
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GenotypeDepth
all individuals: 162
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GenotypeDepth
all individuals: 411
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GenotypeDepth
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GenotypeDepth
all individuals: 314
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GenotypeDepth
all individuals: 81
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GenotypeDepth
all individuals: 10125
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
all individuals: 2341
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 44
bin: 5.75e1
variant carriers: 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: 8652
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
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: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.95e-1

FS
type: SiteQuality
SIO_000300: 5.783e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.57e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.237271e6

QD
type: SiteQuality
SIO_000300: 1.225e1

GenotypeDepth
all individuals: 162
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variant carriers: 1

GenotypeDepth
all individuals: 4233
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variant carriers: 0

GenotypeDepth
all individuals: 393
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variant carriers: 0

GenotypeDepth
all individuals: 15656
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GenotypeDepth
all individuals: 190
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GenotypeDepth
all individuals: 14002
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GenotypeDepth
all individuals: 6497
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variant carriers: 6

GenotypeDepth
all individuals: 69
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GenotypeDepth
all individuals: 414
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GenotypeDepth
all individuals: 80
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GenotypeDepth
all individuals: 262
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variant carriers: 3

GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 156
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GenotypeQuality
all individuals: 275
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GenotypeQuality
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GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 28

GenotypeQuality
all individuals: 3649
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.730403183941858e-4
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 24
allele frequency: 2.311248073959939e-3
allele num: 10384
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-3

FS
type: SiteQuality
SIO_000300: 7.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

DP
type: SiteQuality
SIO_000300: 2.235122e6

QD
type: SiteQuality
SIO_000300: 1.468e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

GenotypeDepth
all individuals: 97
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variant carriers: 0

GenotypeDepth
all individuals: 2345
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GenotypeDepth
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GenotypeDepth
all individuals: 1011
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GenotypeQuality
all individuals: 120
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GenotypeQuality
all individuals: 231
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GenotypeQuality
all individuals: 8634
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3641
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16403
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 2.75e1
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GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 14880
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2327
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5521
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4646
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.592e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

FS
type: SiteQuality
SIO_000300: 5.458e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.45e-1

DP
type: SiteQuality
SIO_000300: 2.228507e6

GenotypeDepth
all individuals: 636
bin: 6.75e1
variant carriers: 33

GenotypeDepth
all individuals: 97
bin: 8.75e1
variant carriers: 7

GenotypeDepth
all individuals: 1669
bin: 5.75e1
variant carriers: 74

GenotypeDepth
all individuals: 259
bin: 7.75e1
variant carriers: 13

GenotypeQuality
all individuals: 5926
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15689
bin: 9.75e1
variant carriers: 1252

GenotypeQuality
all individuals: 1887
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2328
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 8807
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1330
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3047
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 743
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1371
bin: 4.25e1
variant carriers: 2

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

GenotypeQuality
all individuals: 5042
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 4470
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2750
bin: 4.75e1
variant carriers: 2

Latino
type: Population
allele count: 68
allele frequency: 5.908932916232186e-3
allele num: 11508
num of homozygotes: 0

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

Other
type: Population
allele count: 5
allele frequency: 5.518763796909493e-3
allele num: 906
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.505298651252408e-4
allele num: 66432
num of homozygotes: 0

African
type: Population
allele count: 1273
allele frequency: 1.231379377055523e-1
allele num: 10338
num of homozygotes: 75

South Asian
type: Population
allele count: 3
allele frequency: 1.820609297244811e-4
allele num: 16478
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.507e0

DP
type: SiteQuality
SIO_000300: 2.12797e6

VQSLOD
type: SiteQuality
SIO_000300: 5.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.514e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.690000000000001e-2

GenotypeDepth
all individuals: 162
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 307
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 993
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5091
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4522
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3583
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9217
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variant carriers: 0

GenotypeQuality
all individuals: 14815
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1387
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2872
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5921
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2381
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507068149621726e-5
allele num: 66354
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

QD
type: SiteQuality
SIO_000300: 1.239e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-2

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 2.121787e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.29e-1

FS
type: SiteQuality
SIO_000300: 2.019e0

GenotypeDepth
all individuals: 992
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3639
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 11001
bin: 3.25e1
variant carriers: 8

GenotypeDepth
all individuals: 1638
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5771
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4539
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8204
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
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variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5118
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2978
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3580
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14850
bin: 9.75e1
variant carriers: 53

GenotypeQuality
all individuals: 3149
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.605071205279611e-4
allele num: 11516
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 49
allele frequency: 7.383521186185281e-4
allele num: 66364
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.117628e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.497e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

GenotypeDepth
all individuals: 1638
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 307
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 994
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1877
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6806
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3000
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14818
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 680
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 5113
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3620
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3586
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1973
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
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variant carriers: 0

GenotypeQuality
all individuals: 2255
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variant carriers: 0

GenotypeQuality
all individuals: 5635
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variant carriers: 0

GenotypeQuality
all individuals: 1398
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4540
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.02918123718799e-5
allele num: 66344
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 2.116746e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.5e-2

FS
type: SiteQuality
SIO_000300: 1.597e0

QD
type: SiteQuality
SIO_000300: 1.691e1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e-1

GenotypeQuality
all individuals: 1834
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531065315246348e-5
allele num: 65314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14238
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -7.819e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

FS
type: SiteQuality
SIO_000300: 7.928e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.906e1

QD
type: SiteQuality
SIO_000300: 1.023e1

DP
type: SiteQuality
SIO_000300: 3.688296e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.79e-1

GenotypeQuality
all individuals: 663
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65332
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.978630787495053e-4
allele num: 10108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14240
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.387e0

DP
type: SiteQuality
SIO_000300: 3.688816e6

FS
type: SiteQuality
SIO_000300: 6.692e0

QD
type: SiteQuality
SIO_000300: 1.151e1

MQRankSum
type: SiteQuality
SIO_000300: -8.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.01e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.942e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.85e-1

GenotypeQuality
all individuals: 788
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530549773478634e-5
allele num: 65336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14254
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.83e-1

FS
type: SiteQuality
SIO_000300: 2.395e0

MQRankSum
type: SiteQuality
SIO_000300: -1.335e0

DP
type: SiteQuality
SIO_000300: 3.689384e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.446e0

QD
type: SiteQuality
SIO_000300: 1.136e1

MQ
type: SiteQuality
SIO_000300: 5.878e1

VQSLOD
type: SiteQuality
SIO_000300: -2.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

GenotypeQuality
all individuals: 2593
bin: 6.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0