4-114436382-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114436382
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114436382
    reference: chr 4
allele count: 2
allele frequency: 2.170185984938909e-5
allele num: 92158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.82-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.697-35T>C
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9194
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7526
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

4-114436384-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114436384
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114436384
    reference: chr 4
allele count: 1
allele frequency: 1.105803255484784e-5
allele num: 90432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.82-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.697-37T>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18852
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

4-114436387-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114436387
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114436387
    reference: chr 4
allele count: 1
allele frequency: 1.174922455117962e-5
allele num: 85112
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.82-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.697-40G>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13024
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-114436393-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114436393
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114436393
    reference: chr 4
allele count: 2
allele frequency: 2.456881725713724e-5
allele num: 81404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.82-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.697-46G>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

4-114436394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114436394
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114436394
    reference: chr 4
allele count: 1
allele frequency: 1.245423070216953e-5
allele num: 80294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.82-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.697-47C>T
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

4-114436395-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114436395
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114436395
    reference: chr 4
allele count: 1
allele frequency: 1.224829748664936e-5
allele num: 81644
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.82-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.697-48T>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11960
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/4-114436398-A-AAAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114436398
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114436401
    reference: chr 4
allele count: 1
allele frequency: 1.246136975376333e-5
allele num: 80248
alternate allele: AAAC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.82-54_82-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.697-54_697-52dupGTT
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13720
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16536
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

4-114438676-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438676
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438675
    reference: chr 4
allele count: 1
allele frequency: 8.409014463504877e-6
allele num: 118920
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.81+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.696+42delC
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12819
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: AG
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD

4-114438678-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438678
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438678
    reference: chr 4
allele count: 1
allele frequency: 8.399126490844953e-6
allele num: 119060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.81+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.696+41T>C
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12873
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8064
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

4-114438679-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438679
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438679
    reference: chr 4
allele count: 1
allele frequency: 8.412551526878102e-6
allele num: 118870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.696+40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.81+40G>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/4-114438681-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438681
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438681
    reference: chr 4
allele count: 4
allele frequency: 3.361853053403036e-5
allele num: 118982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.81+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.696+38T>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

4-114438697-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438697
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438697
    reference: chr 4
allele count: 230
allele frequency: 1.924009971390808e-3
allele num: 119542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.81+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.696+22C>T
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9311
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8052
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11724
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 6.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 2
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

4-114438702-A-AAAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438702
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438705
    reference: chr 4
allele count: 1
allele frequency: 8.349475652928997e-6
allele num: 119768
alternate allele: AAAT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.81+14_81+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.696+14_696+16dupATT
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13671
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/4-114438703-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438703
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438703
    reference: chr 4
allele count: 12
allele frequency: 1.001401962747847e-4
allele num: 119832
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.81+16T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.696+16T>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11772
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

4-114438705-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438705
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438705
    reference: chr 4
allele count: 2
allele frequency: 1.667695078631823e-5
allele num: 119926
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.81+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.696+14A>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum

4-114438707-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438707
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438707
    reference: chr 4
allele count: 1
allele frequency: 8.333055564814507e-6
allele num: 120004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.81+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.696+12C>T
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

4-114438708-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438708
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438708
    reference: chr 4
allele count: 2
allele frequency: 1.666000266560043e-5
allele num: 120048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.81+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.696+11A>T
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP

4-114438728-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438728
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438728
    reference: chr 4
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.687A>G
  hgvsp: ENST00000296402.5:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.687A>G
  hgvsp: ENST00000394522.3:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.687A>G
  hgvsp: ENST00000429180.1:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.687A>G
  hgvsp: ENST00000508738.1:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.687A>G
  hgvsp: ENST00000418639.2:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.687A>G
  hgvsp: ENST00000342666.5:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.72A>G
  hgvsp: ENST00000509594.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.687A>G
  hgvsp: ENST00000454265.2:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.687A>G
  hgvsp: ENST00000379773.2:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.687A>G
  hgvsp: ENST00000511664.1:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.687A>G
  hgvsp: ENST00000394526.2:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.687A>G
  hgvsp: ENST00000514328.1:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.687A>G
  hgvsp: ENST00000394524.3:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.687A>G
  hgvsp: ENST00000505990.1:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.687A>G
  hgvsp: ENST00000515496.1:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly229Gly
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

4-114438733-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438733
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438733
    reference: chr 4
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.682G>A
  hgvsp: ENSP00000424245.1:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.682G>A
  hgvsp: ENSP00000378032.3:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.682G>A
  hgvsp: ENSP00000378034.2:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.682G>A
  hgvsp: ENSP00000415707.1:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.682G>A
  hgvsp: ENSP00000378030.3:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.682G>A
  hgvsp: ENSP00000406131.2:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.682G>A
  hgvsp: ENSP00000339740.5:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.682G>A
  hgvsp: ENSP00000423482.1:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.682G>A
  hgvsp: ENSP00000296402.5:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.682G>A
  hgvsp: ENSP00000422566.1:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.682G>A
  hgvsp: ENSP00000369098.2:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.682G>A
  hgvsp: ENSP00000425824.1:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.682G>A
  hgvsp: ENSP00000415248.2:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.67G>A
  hgvsp: ENSP00000423753.1:p.Ala23Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.682G>A
  hgvsp: ENSP00000423677.1:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala228Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP

4-114438743-C-CTGAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438743
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438747
    reference: chr 4
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: CTGAT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.668_671dupATCA
  hgvsp: ENSP00000406131.2:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.668_671dupATCA
  hgvsp: ENSP00000423482.1:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.668_671dupATCA
  hgvsp: ENSP00000339740.5:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.668_671dupATCA
  hgvsp: ENSP00000415248.2:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.53_56dupATCA
  hgvsp: ENSP00000423753.1:p.Gln20SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.668_671dupATCA
  hgvsp: ENSP00000415707.1:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.668_671dupATCA
  hgvsp: ENSP00000425824.1:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.668_671dupATCA
  hgvsp: ENSP00000296402.5:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.668_671dupATCA
  hgvsp: ENSP00000422566.1:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.668_671dupATCA
  hgvsp: ENSP00000378034.2:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.668_671dupATCA
  hgvsp: ENSP00000378032.3:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.668_671dupATCA
  hgvsp: ENSP00000378030.3:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.668_671dupATCA
  hgvsp: ENSP00000424245.1:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.668_671dupATCA
  hgvsp: ENSP00000369098.2:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.668_671dupATCA
  hgvsp: ENSP00000423677.1:p.Gln225SerfsTer9
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11115
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln225SerfsTer9
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

4-114438794-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438794
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438794
    reference: chr 4
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.621A>C
  hgvsp: ENST00000505990.1:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.621A>C
  hgvsp: ENST00000508738.1:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.621A>C
  hgvsp: ENST00000394526.2:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.621A>C
  hgvsp: ENST00000418639.2:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.621A>C
  hgvsp: ENST00000454265.2:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.621A>C
  hgvsp: ENST00000394522.3:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423753
  ensembl transcript: ENST00000509594
  gene symbol: CAMK2D
  hgvsc: ENST00000509594.1:c.6A>C
  hgvsp: ENST00000509594.1:c.6A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.621A>C
  hgvsp: ENST00000429180.1:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.621A>C
  hgvsp: ENST00000511664.1:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.621A>C
  hgvsp: ENST00000515496.1:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.621A>C
  hgvsp: ENST00000342666.5:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.621A>C
  hgvsp: ENST00000296402.5:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.621A>C
  hgvsp: ENST00000394524.3:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.621A>C
  hgvsp: ENST00000514328.1:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.621A>C
  hgvsp: ENST00000379773.2:c.621A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu207Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

4-114438817-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438817
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438817
    reference: chr 4
allele count: 1
allele frequency: 8.323068215867098e-6
allele num: 120148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.602-4C>T
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.602-4C>T
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

4-114438818-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438818
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438818
    reference: chr 4
allele count: 998
allele frequency: 8.31126434484252e-3
allele num: 120078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.602-5T>C
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 269
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 3.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 13907
  bin: 2.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 9049
  bin: 2.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 11706
  bin: 3.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 4.25e1
  variant carriers: 50
genotype quality: GenotypeQuality
hgvs: c.602-5T>C
num of homozygotes: 45
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

4-114438847-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438847
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438847
    reference: chr 4
allele count: 1
allele frequency: 8.4199181583955e-6
allele num: 118766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.602-34A>C
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

4-114438849-A-ACTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438849
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438852
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 118424
alternate allele: ACTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.602-37_602-36insAAG
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD

4-114438852-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114438852
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114438852
    reference: chr 4
allele count: 1
allele frequency: 8.457231778894133e-6
allele num: 118242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.602-39A>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7959
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD

4-114452332-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452332
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452332
    reference: chr 4
allele count: 1
allele frequency: 8.416658250008417e-6
allele num: 118812
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.601+40A>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ

4-114452339-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452339
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452339
    reference: chr 4
allele count: 1
allele frequency: 8.4088730428348e-6
allele num: 118922
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.601+33A>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16761
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

4-114452344-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452344
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452344
    reference: chr 4
allele count: 1
allele frequency: 8.39433214693439e-6
allele num: 119128
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.601+28T>C
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD

4-114452350-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452350
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452350
    reference: chr 4
allele count: 2
allele frequency: 1.676530252988415e-5
allele num: 119294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.601+22C>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

4-114452358-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452358
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452358
    reference: chr 4
allele count: 1
allele frequency: 8.356173541012099e-6
allele num: 119672
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.601+14T>C
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

4-114452362-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452362
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452362
    reference: chr 4
allele count: 11
allele frequency: 9.178445671945663e-5
allele num: 119846
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.601+10T>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18370
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/4-114452367-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452367
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452367
    reference: chr 4
allele count: 1
allele frequency: 8.330417687142833e-6
allele num: 120042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.601+5G>T
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.601+5G>T
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

4-114452371-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452371
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452371
    reference: chr 4
allele count: 1
allele frequency: 8.319467554076538e-6
allele num: 120200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.601+1G>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.601+1G>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

4-114452383-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452383
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452383
    reference: chr 4
allele count: 1
allele frequency: 8.303027283747654e-6
allele num: 120438
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.590T>C
  hgvsp: ENSP00000415707.1:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.590T>C
  hgvsp: ENSP00000422566.1:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.590T>C
  hgvsp: ENSP00000423677.1:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.590T>C
  hgvsp: ENSP00000406131.2:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.590T>C
  hgvsp: ENSP00000339740.5:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.590T>C
  hgvsp: ENSP00000415248.2:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.590T>C
  hgvsp: ENSP00000378032.3:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.590T>C
  hgvsp: ENSP00000378030.3:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.590T>C
  hgvsp: ENSP00000425824.1:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.590T>C
  hgvsp: ENSP00000378034.2:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.590T>C
  hgvsp: ENSP00000423482.1:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.590T>C
  hgvsp: ENSP00000424245.1:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.590T>C
  hgvsp: ENSP00000296402.5:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.590T>C
  hgvsp: ENSP00000369098.2:p.Met197Thr
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met197Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

4-114452402-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452402
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452402
    reference: chr 4
allele count: 1
allele frequency: 8.30357884248111e-6
allele num: 120430
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.571T>C
  hgvsp: ENSP00000425824.1:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.571T>C
  hgvsp: ENSP00000415248.2:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.571T>C
  hgvsp: ENSP00000378032.3:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.571T>C
  hgvsp: ENSP00000369098.2:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.571T>C
  hgvsp: ENSP00000378030.3:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.571T>C
  hgvsp: ENSP00000422566.1:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.571T>C
  hgvsp: ENSP00000378034.2:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.571T>C
  hgvsp: ENSP00000424245.1:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.571T>C
  hgvsp: ENSP00000296402.5:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.571T>C
  hgvsp: ENSP00000339740.5:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.571T>C
  hgvsp: ENSP00000406131.2:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.571T>C
  hgvsp: ENSP00000423677.1:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.571T>C
  hgvsp: ENSP00000415707.1:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.571T>C
  hgvsp: ENSP00000423482.1:p.Tyr191His
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr191His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

4-114452404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452404
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452404
    reference: chr 4
allele count: 1
allele frequency: 8.304958059961797e-6
allele num: 120410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.569C>T
  hgvsp: ENSP00000378032.3:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.569C>T
  hgvsp: ENSP00000424245.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.569C>T
  hgvsp: ENSP00000423482.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.569C>T
  hgvsp: ENSP00000422566.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.569C>T
  hgvsp: ENSP00000339740.5:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.569C>T
  hgvsp: ENSP00000423677.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.569C>T
  hgvsp: ENSP00000425824.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.569C>T
  hgvsp: ENSP00000369098.2:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.569C>T
  hgvsp: ENSP00000378034.2:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.569C>T
  hgvsp: ENSP00000406131.2:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.569C>T
  hgvsp: ENSP00000415248.2:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.569C>T
  hgvsp: ENSP00000415707.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.569C>T
  hgvsp: ENSP00000296402.5:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.569C>T
  hgvsp: ENSP00000378030.3:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro190Leu
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

4-114452419-A-ACTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452419
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452422
    reference: chr 4
allele count: 1
allele frequency: 8.327365388138501e-6
allele num: 120086
alternate allele: ACTT
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.551_553dupAAG
  hgvsp: ENSP00000423482.1:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.551_553dupAAG
  hgvsp: ENSP00000296402.5:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.551_553dupAAG
  hgvsp: ENSP00000425824.1:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.551_553dupAAG
  hgvsp: ENSP00000415707.1:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.551_553dupAAG
  hgvsp: ENSP00000406131.2:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.551_553dupAAG
  hgvsp: ENSP00000339740.5:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.551_553dupAAG
  hgvsp: ENSP00000415248.2:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.551_553dupAAG
  hgvsp: ENSP00000424245.1:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.551_553dupAAG
  hgvsp: ENSP00000422566.1:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.551_553dupAAG
  hgvsp: ENSP00000378034.2:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.551_553dupAAG
  hgvsp: ENSP00000378030.3:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.551_553dupAAG
  hgvsp: ENSP00000423677.1:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.551_553dupAAG
  hgvsp: ENSP00000378032.3:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.551_553dupAAG
  hgvsp: ENSP00000369098.2:p.Glu184dup
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19385
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu184dup
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

4-114452420-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452420
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452420
    reference: chr 4
allele count: 1
allele frequency: 8.327226700419692e-6
allele num: 120088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.553G>A
  hgvsp: ENSP00000415707.1:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.553G>A
  hgvsp: ENSP00000425824.1:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.553G>A
  hgvsp: ENSP00000422566.1:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.553G>A
  hgvsp: ENSP00000339740.5:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.553G>A
  hgvsp: ENSP00000424245.1:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.553G>A
  hgvsp: ENSP00000369098.2:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.553G>A
  hgvsp: ENSP00000406131.2:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.553G>A
  hgvsp: ENSP00000423482.1:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.553G>A
  hgvsp: ENSP00000415248.2:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.553G>A
  hgvsp: ENSP00000423677.1:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.553G>A
  hgvsp: ENSP00000378032.3:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.553G>A
  hgvsp: ENSP00000378034.2:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.553G>A
  hgvsp: ENSP00000378030.3:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.553G>A
  hgvsp: ENSP00000296402.5:p.Val185Ile
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19383
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val185Ile
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

4-114452440-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452440
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452440
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 118804
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.533C>A
  hgvsp: ENSP00000424245.1:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.533C>A
  hgvsp: ENSP00000423482.1:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.533C>A
  hgvsp: ENSP00000369098.2:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.533C>A
  hgvsp: ENSP00000378034.2:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.533C>A
  hgvsp: ENSP00000406131.2:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.533C>A
  hgvsp: ENSP00000339740.5:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.533C>A
  hgvsp: ENSP00000422566.1:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.533C>A
  hgvsp: ENSP00000415707.1:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.533C>A
  hgvsp: ENSP00000378030.3:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.533C>A
  hgvsp: ENSP00000415248.2:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.533C>A
  hgvsp: ENSP00000425824.1:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.533C>A
  hgvsp: ENSP00000296402.5:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.533C>A
  hgvsp: ENSP00000423677.1:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.533C>A
  hgvsp: ENSP00000378032.3:p.Pro178His
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 19196
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro178His
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

4-114452445-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452445
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452445
    reference: chr 4
allele count: 1
allele frequency: 8.451942256330504e-6
allele num: 118316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.528C>T
  hgvsp: ENST00000515496.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.528C>T
  hgvsp: ENST00000296402.5:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.528C>T
  hgvsp: ENST00000508738.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.528C>T
  hgvsp: ENST00000379773.2:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.528C>T
  hgvsp: ENST00000394522.3:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.528C>T
  hgvsp: ENST00000394524.3:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.528C>T
  hgvsp: ENST00000418639.2:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.528C>T
  hgvsp: ENST00000394526.2:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.528C>T
  hgvsp: ENST00000342666.5:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.528C>T
  hgvsp: ENST00000505990.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.528C>T
  hgvsp: ENST00000514328.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.528C>T
  hgvsp: ENST00000429180.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.528C>T
  hgvsp: ENST00000454265.2:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.528C>T
  hgvsp: ENST00000511664.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly176Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

4-114452448-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452448
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452448
    reference: chr 4
allele count: 1
allele frequency: 8.487667419239845e-6
allele num: 117818
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.525T>C
  hgvsp: ENST00000508738.1:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.525T>C
  hgvsp: ENST00000394522.3:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.525T>C
  hgvsp: ENST00000418639.2:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.525T>C
  hgvsp: ENST00000429180.1:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.525T>C
  hgvsp: ENST00000515496.1:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.525T>C
  hgvsp: ENST00000379773.2:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.525T>C
  hgvsp: ENST00000394526.2:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.525T>C
  hgvsp: ENST00000505990.1:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.525T>C
  hgvsp: ENST00000296402.5:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.525T>C
  hgvsp: ENST00000514328.1:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.525T>C
  hgvsp: ENST00000454265.2:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.525T>C
  hgvsp: ENST00000342666.5:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.525T>C
  hgvsp: ENST00000394524.3:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.525T>C
  hgvsp: ENST00000511664.1:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18737
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala175Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ

4-114452454-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452454
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452454
    reference: chr 4
allele count: 1
allele frequency: 8.532714427113554e-6
allele num: 117196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.519T>A
  hgvsp: ENST00000511664.1:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.519T>A
  hgvsp: ENST00000394526.2:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.519T>A
  hgvsp: ENST00000454265.2:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.519T>A
  hgvsp: ENST00000418639.2:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.519T>A
  hgvsp: ENST00000342666.5:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.519T>A
  hgvsp: ENST00000515496.1:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.519T>A
  hgvsp: ENST00000514328.1:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.519T>A
  hgvsp: ENST00000505990.1:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.519T>A
  hgvsp: ENST00000379773.2:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.519T>A
  hgvsp: ENST00000394524.3:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.519T>A
  hgvsp: ENST00000394522.3:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.519T>A
  hgvsp: ENST00000508738.1:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.519T>A
  hgvsp: ENST00000429180.1:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.519T>A
  hgvsp: ENST00000296402.5:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.519T>A
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

4-114452459-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452459
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452459
    reference: chr 4
allele count: 1
allele frequency: 8.567365192508696e-6
allele num: 116722
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-4C>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.518-4C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

4-114452468-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452468
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452468
    reference: chr 4
allele count: 1
allele frequency: 8.670620469600805e-6
allele num: 115332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-13C>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18993
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

4-114452470-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452470
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452470
    reference: chr 4
allele count: 2
allele frequency: 1.737076153418566e-5
allele num: 115136
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-15A>C
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/4-114452474-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452474
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452474
    reference: chr 4
allele count: 1
allele frequency: 8.721437292865864e-6
allele num: 114660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-19T>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16692
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-114452476-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452476
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452476
    reference: chr 4
allele count: 1
allele frequency: 8.736523911865946e-6
allele num: 114462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-21A>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9973
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

4-114452477-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452477
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452477
    reference: chr 4
allele count: 1
allele frequency: 8.744774996939329e-6
allele num: 114354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-22C>T
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10000
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

4-114452477-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452477
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452477
    reference: chr 4
allele count: 1
allele frequency: 8.744774996939329e-6
allele num: 114354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-22C>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15733
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

4-114452481-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452481
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452481
    reference: chr 4
allele count: 3
allele frequency: 2.637130801687764e-5
allele num: 113760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-26G>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13435
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-114452483-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452483
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452483
    reference: chr 4
allele count: 1
allele frequency: 8.807003329047259e-6
allele num: 113546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-28G>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12662
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

4-114452490-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452490
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452490
    reference: chr 4
allele count: 1
allele frequency: 8.876264867743653e-6
allele num: 112660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-35A>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13803
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: T
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-114452495-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452495
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452495
    reference: chr 4
allele count: 1
allele frequency: 9.003169115528666e-6
allele num: 111072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-40G>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13361
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

4-114452504-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114452504
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114452505
    reference: chr 4
allele count: 1
allele frequency: 9.310466826806695e-6
allele num: 107406
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.518-50dupA
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13022
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

4-114458453-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114458453
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114458453
    reference: chr 4
allele count: 1
allele frequency: 8.321959988016378e-6
allele num: 120164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.517+44T>C
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11534
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

4-114458466-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114458466
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114458466
    reference: chr 4
allele count: 1
allele frequency: 8.310203267571925e-6
allele num: 120334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.517+31A>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11879
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: T
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-114458469-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114458469
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114458469
    reference: chr 4
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.517+28C>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum

4-114458477-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114458477
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114458477
    reference: chr 4
allele count: 1
allele frequency: 8.291048983517394e-6
allele num: 120612
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.517+20T>C
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16498
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

4-114458483-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114458483
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114458483
    reference: chr 4
allele count: 1
allele frequency: 8.283219853221344e-6
allele num: 120726
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.517+14C>G
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12187
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

4-114458487-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114458487
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114458487
    reference: chr 4
allele count: 1
allele frequency: 8.278145695364238e-6
allele num: 120800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.517+10G>A
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

4-114458503-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114458503
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114458503
    reference: chr 4
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.511T>C
  hgvsp: ENSP00000339740.5:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.511T>C
  hgvsp: ENSP00000415248.2:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.511T>C
  hgvsp: ENSP00000296402.5:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.511T>C
  hgvsp: ENSP00000425824.1:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.511T>C
  hgvsp: ENSP00000423677.1:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.511T>C
  hgvsp: ENSP00000406131.2:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.511T>C
  hgvsp: ENSP00000369098.2:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.511T>C
  hgvsp: ENSP00000378034.2:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.511T>C
  hgvsp: ENSP00000415707.1:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.511T>C
  hgvsp: ENSP00000378030.3:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.511T>C
  hgvsp: ENSP00000378032.3:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.511T>C
  hgvsp: ENSP00000423482.1:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.511T>C
  hgvsp: ENSP00000422566.1:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.511T>C
  hgvsp: ENSP00000424245.1:p.Trp171Arg
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp171Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

4-114458504-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114458504
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114458504
    reference: chr 4
allele count: 3
allele frequency: 2.479297862845242e-5
allele num: 121002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.510G>A
  hgvsp: ENST00000379773.2:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.510G>A
  hgvsp: ENST00000394522.3:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.510G>A
  hgvsp: ENST00000394524.3:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.510G>A
  hgvsp: ENST00000505990.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.510G>A
  hgvsp: ENST00000342666.5:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.510G>A
  hgvsp: ENST00000296402.5:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.510G>A
  hgvsp: ENST00000429180.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.510G>A
  hgvsp: ENST00000511664.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.510G>A
  hgvsp: ENST00000418639.2:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.510G>A
  hgvsp: ENST00000454265.2:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.510G>A
  hgvsp: ENST00000508738.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.510G>A
  hgvsp: ENST00000515496.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.510G>A
  hgvsp: ENST00000394526.2:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.510G>A
  hgvsp: ENST00000514328.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12357
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala170Ala
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

4-114458511-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114458511
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114458511
    reference: chr 4
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.503A>T
  hgvsp: ENSP00000424245.1:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.503A>T
  hgvsp: ENSP00000422566.1:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.503A>T
  hgvsp: ENSP00000425824.1:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.503A>T
  hgvsp: ENSP00000415248.2:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.503A>T
  hgvsp: ENSP00000415707.1:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.503A>T
  hgvsp: ENSP00000339740.5:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.503A>T
  hgvsp: ENSP00000423677.1:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.503A>T
  hgvsp: ENSP00000378034.2:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.503A>T
  hgvsp: ENSP00000423482.1:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.503A>T
  hgvsp: ENSP00000406131.2:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.503A>T
  hgvsp: ENSP00000378032.3:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.503A>T
  hgvsp: ENSP00000378030.3:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.503A>T
  hgvsp: ENSP00000296402.5:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.503A>T
  hgvsp: ENSP00000369098.2:p.Gln168Leu
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln168Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

4-114458513-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114458513
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 114458513
    reference: chr 4
allele count: 692
allele frequency: 5.715701660196581e-3
allele num: 121070
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415707
  ensembl transcript: ENST00000429180
  gene symbol: CAMK2D
  hgvsc: ENST00000429180.1:c.501C>A
  hgvsp: ENSP00000415707.1:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378032
  ensembl transcript: ENST00000394524
  gene symbol: CAMK2D
  hgvsc: ENST00000394524.3:c.501C>A
  hgvsp: ENSP00000378032.3:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000424245
  ensembl transcript: ENST00000505990
  gene symbol: CAMK2D
  hgvsc: ENST00000505990.1:c.501C>A
  hgvsp: ENSP00000424245.1:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423677
  ensembl transcript: ENST00000514328
  gene symbol: CAMK2D
  hgvsc: ENST00000514328.1:c.501C>A
  hgvsp: ENSP00000423677.1:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000425824
  ensembl transcript: ENST00000511664
  gene symbol: CAMK2D
  hgvsc: ENST00000511664.1:c.501C>A
  hgvsp: ENSP00000425824.1:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378034
  ensembl transcript: ENST00000394526
  gene symbol: CAMK2D
  hgvsc: ENST00000394526.2:c.501C>A
  hgvsp: ENSP00000378034.2:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000423482
  ensembl transcript: ENST00000515496
  gene symbol: CAMK2D
  hgvsc: ENST00000515496.1:c.501C>A
  hgvsp: ENSP00000423482.1:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000378030
  ensembl transcript: ENST00000394522
  gene symbol: CAMK2D
  hgvsc: ENST00000394522.3:c.501C>A
  hgvsp: ENSP00000378030.3:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000422566
  ensembl transcript: ENST00000508738
  gene symbol: CAMK2D
  hgvsc: ENST00000508738.1:c.501C>A
  hgvsp: ENSP00000422566.1:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000339740
  ensembl transcript: ENST00000342666
  gene symbol: CAMK2D
  hgvsc: ENST00000342666.5:c.501C>A
  hgvsp: ENSP00000339740.5:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000415248
  ensembl transcript: ENST00000454265
  gene symbol: CAMK2D
  hgvsc: ENST00000454265.2:c.501C>A
  hgvsp: ENSP00000415248.2:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000406131
  ensembl transcript: ENST00000418639
  gene symbol: CAMK2D
  hgvsc: ENST00000418639.2:c.501C>A
  hgvsp: ENSP00000406131.2:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000296402
  ensembl transcript: ENST00000296402
  gene symbol: CAMK2D
  hgvsc: ENST00000296402.5:c.501C>A
  hgvsp: ENSP00000296402.5:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145349
  ensembl protein: ENSP00000369098
  ensembl transcript: ENST00000379773
  gene symbol: CAMK2D
  hgvsc: ENST00000379773.2:c.501C>A
  hgvsp: ENSP00000369098.2:p.Asp167Glu
  variant of: http://identifiers.org/hgnc/1462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 16240
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.25e1
  variant carriers: 28
genotype quality: GenotypeQuality
hgvs: p.Asp167Glu
num of homozygotes: 2
reference allele: G

GenotypeDepth
all individuals: 265
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19294
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 523
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10464
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1464
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5144
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4056
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17315
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4644
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6607
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2649
bin: 9.75e1
variant carriers: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.96935656730044e-5
allele num: 50386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5316
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.669e1

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.59e0

DP
type: SiteQuality
SIO_000300: 1.102559e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

GenotypeDepth
all individuals: 4807
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 927
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 351
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5392
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16256
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1552
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1678
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5035
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7233
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4840
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1601
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7577
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2644
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.02232648438764e-5
allele num: 49448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.96e0

MQ
type: SiteQuality
SIO_000300: 3.793e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.054697e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.068e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

GenotypeDepth
all individuals: 156
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11311
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1888
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 98
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13896
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4760
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2529
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2988
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5576
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7325
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5639
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2643
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 400
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2649
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7092
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.144634125418203e-5
allele num: 46628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4950
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.005057e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

QD
type: SiteQuality
SIO_000300: 1.405e1

MQ
type: SiteQuality
SIO_000300: 5.932e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.766e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.19e-1

GenotypeDepth
all individuals: 262
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16891
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5088
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 93
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7236
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3435
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13010
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5607
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4684
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2277
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2639
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5796
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3804
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.087192868014786e-4
allele num: 9198
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10996
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.234736748011084e-5
allele num: 44748
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 9.7635e5

QD
type: SiteQuality
SIO_000300: 9.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

GenotypeDepth
all individuals: 5180
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 262
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13325
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 343
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3135
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7274
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3131
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4676
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5722
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4090
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12236
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3137
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2638
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5599
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.266545784224841e-5
allele num: 44120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10878
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4722
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-2

QD
type: SiteQuality
SIO_000300: 9.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.423e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.55e-2

DP
type: SiteQuality
SIO_000300: 9.69425e5

GenotypeDepth
all individuals: 93
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 193
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5206
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1157
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 341
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5659
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3037
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3903
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3485
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2638
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 167
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5699
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12703
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3083
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4751
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7451
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4772
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4160
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.078748651564186e-4
allele num: 9270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11112
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.262e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.23e-2

DP
type: SiteQuality
SIO_000300: 9.67316e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1116
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5805
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1398
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5695
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2639
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3140
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4734
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2313
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 986
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4940
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3225
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11532
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 350
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7381
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5467
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2685
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4706
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4064
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6756
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.090750436300175e-4
allele num: 9168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44062
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.261e1

MQRankSum
type: SiteQuality
SIO_000300: -1.568e0

QD
type: SiteQuality
SIO_000300: 7.79e0

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

DP
type: SiteQuality
SIO_000300: 9.63583e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.036e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.37e-2

GenotypeDepth
all individuals: 292
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8046
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5222
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1170
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 368
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 785
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6555
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3277
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 468
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14929
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15152
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4773
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515656734062869e-5
allele num: 65978
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.04e1

DP
type: SiteQuality
SIO_000300: 2.084524e6

QD
type: SiteQuality
SIO_000300: 2.05e1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

GenotypeDepth
all individuals: 1041
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 792
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2510
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 444
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 368
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1170
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5217
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6597
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 543
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15164
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4795
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3193
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4180
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15160
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514417252241338e-5
allele num: 66032
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15104
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

DP
type: SiteQuality
SIO_000300: 2.086711e6

MQRankSum
type: SiteQuality
SIO_000300: -1.308e0

FS
type: SiteQuality
SIO_000300: 4.624e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

QD
type: SiteQuality
SIO_000300: 7.53e0

GenotypeDepth
all individuals: 8063
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1170
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1929
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7510
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5222
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 15405
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15149
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 538
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3171
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 376
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3267
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6561
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1066
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65972
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14988
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.19e0

DP
type: SiteQuality
SIO_000300: 2.088463e6

MQRankSum
type: SiteQuality
SIO_000300: -6.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.688e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

GenotypeDepth
all individuals: 292
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12975
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1169
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8063
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 792
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 785
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 445
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3268
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3174
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15828
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 617
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15153
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 6583
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4758
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.06060606060606e-5
allele num: 66000
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15066
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.049e0

FS
type: SiteQuality
SIO_000300: 7.423e0

QD
type: SiteQuality
SIO_000300: 1.878e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e0

VQSLOD
type: SiteQuality
SIO_000300: -1.135e0

DP
type: SiteQuality
SIO_000300: 2.090911e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeDepth
all individuals: 857
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 581
bin: 1.75e1
variant carriers: 5

GenotypeDepth
all individuals: 13505
bin: 2.75e1
variant carriers: 13

GenotypeDepth
all individuals: 5224
bin: 4.25e1
variant carriers: 19

GenotypeDepth
all individuals: 1398
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1187
bin: 5.75e1
variant carriers: 18

GenotypeDepth
all individuals: 178
bin: 9.25e1
variant carriers: 3

GenotypeDepth
all individuals: 375
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 473
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15274
bin: 9.75e1
variant carriers: 226

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18101
bin: 6.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4733
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6677
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.359722012388578e-4
allele num: 66190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Latino
type: Population
allele count: 17
allele frequency: 1.474670367800139e-3
allele num: 11528
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: 203
allele frequency: 1.959837806526357e-2
allele num: 10358
num of homozygotes: 2

South Asian
type: Population
allele count: 1
allele frequency: 6.509569066527795e-5
allele num: 15362
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.549e0

FS
type: SiteQuality
SIO_000300: 8.05e-1

QD
type: SiteQuality
SIO_000300: 1.179e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.81e-2

MQ
type: SiteQuality
SIO_000300: 5.981e1

DP
type: SiteQuality
SIO_000300: 2.118539e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

GenotypeDepth
all individuals: 11770
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1931
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1175
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1085
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2181
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18853
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15117
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4180
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6733
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66256
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.456611570247934e-5
allele num: 15488
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

DP
type: SiteQuality
SIO_000300: 2.118353e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.5e-1

MQ
type: SiteQuality
SIO_000300: 5.65e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

GenotypeDepth
all individuals: 13684
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1928
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 774
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 369
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 792
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3175
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15120
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6736
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18872
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4177
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66272
num of homozygotes: 0

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

East Asian
type: Population
allele count: 12
allele frequency: 1.391143055877579e-3
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15528
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

DP
type: SiteQuality
SIO_000300: 2.119899e6

QD
type: SiteQuality
SIO_000300: 1.602e1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeDepth
all individuals: 770
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 906
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13727
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1927
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3179
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4184
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6758
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15112
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 19134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508341126429153e-5
allele num: 66298
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15584
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

QD
type: SiteQuality
SIO_000300: 2.001e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.121781e6

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: -5.615e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.637e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.14e0

GenotypeDepth
all individuals: 5226
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10203
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8073
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11788
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 450
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 791
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6763
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3180
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15112
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19298
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66316
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.397134083930399e-5
allele num: 15632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.123841e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 5.869e1

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.556e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.281e0

QD
type: SiteQuality
SIO_000300: 1.088e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.9e-2

GenotypeDepth
all individuals: 449
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13780
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11792
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 756
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 369
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19391
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3182
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15113
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6766
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66330
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.732801940738174e-4
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15664
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

QD
type: SiteQuality
SIO_000300: 1.324e1

VQSLOD
type: SiteQuality
SIO_000300: 7.95e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

DP
type: SiteQuality
SIO_000300: 2.124964e6

GenotypeDepth
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14204
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3158
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11861
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2179
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4184
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20683
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3188
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15111
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6850
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

FS
type: SiteQuality
SIO_000300: 6.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.91e-1

QD
type: SiteQuality
SIO_000300: 1.293e1

DP
type: SiteQuality
SIO_000300: 2.141215e6

GenotypeDepth
all individuals: 293
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14261
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 368
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1928
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11080
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 449
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6862
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4182
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15111
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20821
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3190
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2179
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.207e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.147e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.756e0

QD
type: SiteQuality
SIO_000300: 1.057e1

MQRankSum
type: SiteQuality
SIO_000300: -8.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 2.024e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.35e0

DP
type: SiteQuality
SIO_000300: 2.14306e6

GenotypeDepth
all individuals: 769
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5224
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1174
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1928
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3158
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4182
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15110
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4760
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2179
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20918
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6870
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.853e0

DP
type: SiteQuality
SIO_000300: 2.144727e6

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 8.065e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.68e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.63e-1

QD
type: SiteQuality
SIO_000300: 1.462e1

GenotypeDepth
all individuals: 11871
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3159
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 368
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1174
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 449
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1929
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20660
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6845
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4737
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15111
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.618e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.26e-1

FS
type: SiteQuality
SIO_000300: 4.239e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: -7.492e-1

DP
type: SiteQuality
SIO_000300: 2.141833e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.87e-1

QD
type: SiteQuality
SIO_000300: 1.6e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 368
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1930
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11821
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3159
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1174
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1332
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4175
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18789
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6736
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15111
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4727
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3164
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15918
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507295309296997e-5
allele num: 66344
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.713e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.58e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.121413e6

FS
type: SiteQuality
SIO_000300: 1.778e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 1.506e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

GenotypeDepth
all individuals: 210
bin: 9.25e1
variant carriers: 48

GenotypeDepth
all individuals: 446
bin: 1.75e1
variant carriers: 11

GenotypeDepth
all individuals: 591
bin: 6.75e1
variant carriers: 39

GenotypeDepth
all individuals: 1184
bin: 5.75e1
variant carriers: 47

GenotypeDepth
all individuals: 1932
bin: 5.25e1
variant carriers: 55

GenotypeDepth
all individuals: 294
bin: 8.75e1
variant carriers: 60

GenotypeDepth
all individuals: 478
bin: 7.25e1
variant carriers: 49

GenotypeDepth
all individuals: 3128
bin: 4.75e1
variant carriers: 46

GenotypeDepth
all individuals: 616
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 1428
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4669
bin: 7.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 418
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 15511
bin: 9.75e1
variant carriers: 943

GenotypeQuality
all individuals: 204
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3218
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 4124
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6662
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3126
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 348
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18372
bin: 6.25e1
variant carriers: 1

African
type: Population
allele count: 940
allele frequency: 9.174311926605505e-2
allele num: 10246
num of homozygotes: 45

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

South Asian
type: Population
allele count: 5
allele frequency: 3.14821810855056e-4
allele num: 15882
num of homozygotes: 0

Latino
type: Population
allele count: 40
allele frequency: 3.471017007983339e-3
allele num: 11524
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.960311237107184e-4
allele num: 66316
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.44e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

QD
type: SiteQuality
SIO_000300: 1.559e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.95e-2

DP
type: SiteQuality
SIO_000300: 2.148699e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.71e-1

FS
type: SiteQuality
SIO_000300: 7.77e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeDepth
all individuals: 787
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 713
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1171
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2179
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13838
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1019
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2423
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4674
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14868
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4148
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3249
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6236
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
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: 1
allele frequency: 9.970089730807577e-5
allele num: 10030
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65930
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e-1

FS
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.057326e6

QD
type: SiteQuality
SIO_000300: 8.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

GenotypeDepth
all individuals: 353
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3132
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3463
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 444
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1171
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4633
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2441
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 180
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 703
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14858
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6128
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13232
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4125
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1536
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3243
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15106
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65854
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.061e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.52e-1

DP
type: SiteQuality
SIO_000300: 2.051675e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

QD
type: SiteQuality
SIO_000300: 4.6e-1

MQ
type: SiteQuality
SIO_000300: 4.349e1

VQSLOD
type: SiteQuality
SIO_000300: -7.456e-1

GenotypeDepth
all individuals: 5583
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1916
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 443
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2984
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4119
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1880
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2319
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5887
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11522
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14857
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3238
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4635
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15056
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9964
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520034048762692e-5
allele num: 65788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: -6.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.17e1

DP
type: SiteQuality
SIO_000300: 2.038027e6

VQSLOD
type: SiteQuality
SIO_000300: 6.77e-1

GenotypeDepth
all individuals: 1043
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1362
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16015
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2067
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1278
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2106
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2563
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5513
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1828
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5442
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31050
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534212948757288e-5
allele num: 65180
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16222
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 1.67633e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

QD
type: SiteQuality
SIO_000300: 1.048e1

FS
type: SiteQuality
SIO_000300: 1.071e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1043
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5509
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1739
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1269
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1814
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1781
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34259
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5470
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65272
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.74089226573154e-5
allele num: 10266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.411e0

QD
type: SiteQuality
SIO_000300: 1.451e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.103e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: -8.879e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

FS
type: SiteQuality
SIO_000300: 1.226e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 1.703629e6

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1374
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1538
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 583
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1279
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1795
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5540
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1459
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36349
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5507
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 727
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.150061500615006e-5
allele num: 16260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65368
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.81e-1

MQ
type: SiteQuality
SIO_000300: 5.9e1

VQSLOD
type: SiteQuality
SIO_000300: -1.73e-2

DP
type: SiteQuality
SIO_000300: 1.720109e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.187e1

GenotypeDepth
all individuals: 24686
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 836
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1043
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5522
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5509
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1255
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37597
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.054927598215922e-5
allele num: 65468
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.687e0

FS
type: SiteQuality
SIO_000300: 4.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.13e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.734648e6

QD
type: SiteQuality
SIO_000300: 1.324e1

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18262
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5611
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1085
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5507
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 234
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39623
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1269
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16334
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522116350573838e-5
allele num: 65698
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.964e0

FS
type: SiteQuality
SIO_000300: 3.461e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

VQSLOD
type: SiteQuality
SIO_000300: -1.794e0

DP
type: SiteQuality
SIO_000300: 1.750039e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

QD
type: SiteQuality
SIO_000300: 2.006e1

GenotypeDepth
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26365
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1384
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 5438
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5646
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5516
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 824
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40365
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.671681711802073e-4
allele num: 65802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
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: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.1e-2

DP
type: SiteQuality
SIO_000300: 1.756141e6

GenotypeDepth
all individuals: 412
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26791
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 894
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2287
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5673
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1276
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5509
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 379
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41116
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516806212838248e-5
allele num: 65928
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.628e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.855e0

VQSLOD
type: SiteQuality
SIO_000300: -3.262e0

MQRankSum
type: SiteQuality
SIO_000300: -1.95e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.37e0

DP
type: SiteQuality
SIO_000300: 1.762835e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

MQ
type: SiteQuality
SIO_000300: 5.927e1

QD
type: SiteQuality
SIO_000300: 1.24e1

GenotypeDepth
all individuals: 1378
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 532
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 27078
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5701
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5508
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 226
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41351
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51437138443832e-5
allele num: 66034
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.585e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.0e-2

DP
type: SiteQuality
SIO_000300: 1.767045e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.93e-1

QD
type: SiteQuality
SIO_000300: 1.061e1

FS
type: SiteQuality
SIO_000300: 2.564e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 383
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19066
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 135
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1043
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 561
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 565
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1604
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42133
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5506
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510665296996797e-5
allele num: 66196
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.212e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.774389e6

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.133e1

GenotypeDepth
all individuals: 212
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 563
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 444
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 19324
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1042
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5767
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42034
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5505
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1835
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511395925276585e-5
allele num: 66164
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.047e0

DP
type: SiteQuality
SIO_000300: 1.776667e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

QD
type: SiteQuality
SIO_000300: 1.09e1

GenotypeDepth
all individuals: 167
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 836
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2292
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 373
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1835
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5504
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 158
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5755
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41947
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511898642315019e-5
allele num: 66142
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.475e0

DP
type: SiteQuality
SIO_000300: 1.776651e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 2.456e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.504e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.425e0

GenotypeDepth
all individuals: 1042
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1374
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 836
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2289
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 160
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5732
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5503
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1583
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1816
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41533
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65924
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.787e0

DP
type: SiteQuality
SIO_000300: 1.771793e6

MQ
type: SiteQuality
SIO_000300: 5.815e1

MQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.14e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.87e-2

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 585
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1043
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 562
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5517
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41588
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5721
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5502
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 89
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65922
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.674922600619196e-5
allele num: 10336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.772079e6

FS
type: SiteQuality
SIO_000300: 2.268e0

MQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

QD
type: SiteQuality
SIO_000300: 1.616e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.206e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.216e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.67e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.489e-1

MQ
type: SiteQuality
SIO_000300: 5.881e1

GenotypeDepth
all individuals: 317
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 573
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1373
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 837
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1042
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5553
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1771
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1528
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2150
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39536
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5502
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.601e0

DP
type: SiteQuality
SIO_000300: 1.750052e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeDepth
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 681
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2100
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1374
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1043
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 562
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18951
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5503
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38763
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5502
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543352779578356e-5
allele num: 64794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16150
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 1.740053e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.099e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.174e1

FS
type: SiteQuality
SIO_000300: 1.948e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

GenotypeDepth
all individuals: 836
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23370
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2285
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1742
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5421
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3254
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5502
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 585
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549762886278399e-5
allele num: 64526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16072
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.728091e6

VQSLOD
type: SiteQuality
SIO_000300: 1.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.117e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 213
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1375
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22504
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18537
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1987
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 875
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2281
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5501
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 283
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36547
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1705
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5231
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3961
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11284
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.249218847644044e-5
allele num: 16002
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.69e-1

MQ
type: SiteQuality
SIO_000300: 5.988e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 3.469e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.007e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.07e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.088e0

DP
type: SiteQuality
SIO_000300: 1.714581e6

QD
type: SiteQuality
SIO_000300: 1.102e1

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 840
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18330
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1042
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 563
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1372
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5501
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 265
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1234
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4481
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1688
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5137
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.565582240035069e-5
allele num: 63874
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15946
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.704484e6

MQ
type: SiteQuality
SIO_000300: 5.875e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.41e0

FS
type: SiteQuality
SIO_000300: 3.803e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

QD
type: SiteQuality
SIO_000300: 1.625e1

VQSLOD
type: SiteQuality
SIO_000300: -1.596e0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1042
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6736
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5499
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32104
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4813
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6495
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1222
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.011736139214893e-4
allele num: 9884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63056
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8138
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: 6444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15764
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 1.656163e6

QD
type: SiteQuality
SIO_000300: 1.403e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

GenotypeDepth
all individuals: 213
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1371
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31237
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6930
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5499
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4736
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62942
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9854
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.270486596366408e-4
allele num: 15742
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.871e1

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e-1

FS
type: SiteQuality
SIO_000300: 3.183e0

DP
type: SiteQuality
SIO_000300: 1.644614e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

GenotypeDepth
all individuals: 411
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1042
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1369
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7926
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5499
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28990
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1611
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4557
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2629
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1352
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1341
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11100
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15686
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.018537380321858e-4
allele num: 9818
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.558e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.745e0

VQSLOD
type: SiteQuality
SIO_000300: -1.919e0

QD
type: SiteQuality
SIO_000300: 3.44e0

MQRankSum
type: SiteQuality
SIO_000300: -1.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.615587e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.113e0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 837
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8375
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1339
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2996
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5498
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27792
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1583
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1208
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4452
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1601
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62602
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.24750499001996e-4
allele num: 8016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15662
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: -2.081e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

QD
type: SiteQuality
SIO_000300: 6.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

DP
type: SiteQuality
SIO_000300: 1.599772e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 411
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5040
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1206
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4413
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8411
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5499
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27943
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8004
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.598823266076168e-5
allele num: 62546
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.899e1

FS
type: SiteQuality
SIO_000300: 5.212e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.211e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.69e-1

QD
type: SiteQuality
SIO_000300: 1.16e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e-1

DP
type: SiteQuality
SIO_000300: 1.599531e6

GenotypeDepth
all individuals: 15643
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1206
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27943
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5499
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4413
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8411
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.030160736861116e-5
allele num: 11074
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.16e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.211e0

FS
type: SiteQuality
SIO_000300: 5.212e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 5.899e1

VQSLOD
type: SiteQuality
SIO_000300: 2.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e-1

DP
type: SiteQuality
SIO_000300: 1.599531e6

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeDepth
all individuals: 213
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1041
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4876
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9373
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2301
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24369
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5496
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3998
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4151
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2978
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11022
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.820825968182548e-5
allele num: 62230
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15588
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.560135e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e-1

FS
type: SiteQuality
SIO_000300: 3.356e0

QD
type: SiteQuality
SIO_000300: 1.071e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.496e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

GenotypeDepth
all individuals: 833
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 413
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4546
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3268
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2764
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 342
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22498
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9738
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1551
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5494
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4028
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6418
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.425083526085839e-5
allele num: 15564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62068
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -6.538e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.78e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 5.871e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.056e0

DP
type: SiteQuality
SIO_000300: 1.539586e6

GenotypeDepth
all individuals: 317
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11122
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1041
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4254
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3864
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10200
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3635
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1341
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6013
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5492
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61558
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.039933444259567e-4
allele num: 9616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10952
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.483957e6

QD
type: SiteQuality
SIO_000300: 1.753e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.542e-1

FS
type: SiteQuality
SIO_000300: 5.539e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 833
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1041
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1372
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10042
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6773
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2086
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4110
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5616
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3211
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13318
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2061
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5485
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1403
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9476
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.575795776867318e-4
allele num: 6346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60686
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

QD
type: SiteQuality
SIO_000300: 1.508e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.932e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.37e0

DP
type: SiteQuality
SIO_000300: 1.447386e6

GenotypeDepth
all individuals: 1041
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10489
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5270
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5028
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3235
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7195
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4112
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2290
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6715
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7859
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5490
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14926
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.707883590654461e-5
allele num: 58552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9104
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.404589e6

VQSLOD
type: SiteQuality
SIO_000300: -2.414e0

FS
type: SiteQuality
SIO_000300: 1.1434e1

MQ
type: SiteQuality
SIO_000300: 3.527e1

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.214e0

QD
type: SiteQuality
SIO_000300: 2.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.476e0

GenotypeDepth
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1314
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8932
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35634
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2239
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 511
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2289
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2363
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.157635467980295e-5
allele num: 16240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

DP
type: SiteQuality
SIO_000300: 1.671162e6

MQRankSum
type: SiteQuality
SIO_000300: -1.755e0

FS
type: SiteQuality
SIO_000300: 3.245e0

VQSLOD
type: SiteQuality
SIO_000300: -9.467e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.57e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

GenotypeDepth
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 23580
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16185
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3171
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39408
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8983
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2183
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2305
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509206157561123e-5
allele num: 66260
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.752e1

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

FS
type: SiteQuality
SIO_000300: 9.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.8e-1

DP
type: SiteQuality
SIO_000300: 1.698519e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

GenotypeDepth
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11939
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8989
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2303
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39614
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2223
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1228
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50879628232596e-5
allele num: 66278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16316
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

MQRankSum
type: SiteQuality
SIO_000300: 8.65e-1

QD
type: SiteQuality
SIO_000300: 2.788e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.434e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.703333e6

FS
type: SiteQuality
SIO_000300: 6.929e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.39e-1

GenotypeDepth
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 608
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2174
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2220
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40776
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9079
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506387081224391e-5
allele num: 66384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
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: 8590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.715036e6

QD
type: SiteQuality
SIO_000300: 1.306e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e0

VQSLOD
type: SiteQuality
SIO_000300: -1.236e0

MQRankSum
type: SiteQuality
SIO_000300: -2.134e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.38e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

GenotypeDepth
all individuals: 103
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2300
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41106
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2162
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2220
bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505072092953252e-5
allele num: 66442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.098e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.721323e6

FS
type: SiteQuality
SIO_000300: 6.217e0

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.215e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

VQSLOD
type: SiteQuality
SIO_000300: -2.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.15e-1

GenotypeDepth
all individuals: 3216
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41201
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 152
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2220
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 340
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9118
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.758101243650377e-5
allele num: 11418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66458
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.791e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

DP
type: SiteQuality
SIO_000300: 1.724553e6

VQSLOD
type: SiteQuality
SIO_000300: -1.288e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.52e0

QD
type: SiteQuality
SIO_000300: 1.033e1

MQRankSum
type: SiteQuality
SIO_000300: 6.41e-1

FS
type: SiteQuality
SIO_000300: 1.751e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.314e0

GenotypeDepth
all individuals: 148
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24995
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 615
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 230
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41918
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9180
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2167
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 9.25e1
variant carriers: 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: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
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: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.762e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.265e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

DP
type: SiteQuality
SIO_000300: 1.731026e6

QD
type: SiteQuality
SIO_000300: 6.1e0

VQSLOD
type: SiteQuality
SIO_000300: -2.271e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

GenotypeDepth
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25011
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1342
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 140
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2162
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41932
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9178
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50253929140247e-5
allele num: 66554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.08e0

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.32e-1

FS
type: SiteQuality
SIO_000300: 7.54e-1

QD
type: SiteQuality
SIO_000300: 9.99e0

DP
type: SiteQuality
SIO_000300: 1.731613e6

GenotypeDepth
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12371
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3225
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25081
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16366
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9189
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42038
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 206
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.541e-1

QD
type: SiteQuality
SIO_000300: 1.194e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQ
type: SiteQuality
SIO_000300: 5.866e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.813e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.29e-1

DP
type: SiteQuality
SIO_000300: 1.732524e6

GenotypeDepth
all individuals: 24943
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 206
bin: 9.75e1
variant carriers: 66

GenotypeDepth
all individuals: 115
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 7.75e1
variant carriers: 49

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 43

GenotypeDepth
all individuals: 12224
bin: 3.25e1
variant carriers: 7

GenotypeDepth
all individuals: 3143
bin: 3.75e1
variant carriers: 18

GenotypeDepth
all individuals: 51
bin: 9.25e1
variant carriers: 22

GenotypeDepth
all individuals: 626
bin: 4.75e1
variant carriers: 46

GenotypeQuality
all individuals: 550
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9118
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2679
bin: 9.75e1
variant carriers: 689

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0