http://identifiers.org/exac.variant/14-24800386-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800386
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800386
    reference: chr 14
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.818+28G>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.818+28G>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.422+28G>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1277+28G>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.25+28G>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.818+28G>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.349+28G>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.818+28G>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3472
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37945
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS

14-24800391-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800391
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800391
    reference: chr 14
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.818+23G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.25+23G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.818+23G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.349+23G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.818+23G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1277+23G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.818+23G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.422+23G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8376
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

14-24800393-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800393
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800393
    reference: chr 14
allele count: 2
allele frequency: 1.651554938975045e-5
allele num: 121098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.818+21A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.422+21A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.25+21A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.349+21A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1277+21A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.818+21A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.818+21A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.818+21A>G
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38270
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-24800397-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800397
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800397
    reference: chr 14
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1277+17C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.818+17C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.422+17C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.818+17C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.818+17C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.818+17C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.25+17C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.349+17C>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8383
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2379
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

14-24800407-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800407
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800407
    reference: chr 14
allele count: 3
allele frequency: 2.473288484368817e-5
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.422+7G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.25+7G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.818+7G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.818+7G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.818+7G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1277+7G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.349+7G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.818+7G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 8.75e1
  variant carriers: 0
hgvs: c.818+7G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-24800410-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800410
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800410
    reference: chr 14
allele count: 3
allele frequency: 2.472880741204788e-5
allele num: 121316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.349+4T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.818+4T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1277+4T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.25+4T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.818+4T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.818+4T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.818+4T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.422+4T>G
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2213
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8419
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38914
  bin: 6.25e1
  variant carriers: 0
hgvs: c.818+4T>G
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

14-24800410-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800410
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800410
    reference: chr 14
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.818+4T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.818+4T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.818+4T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.422+4T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.818+4T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.25+4T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1277+4T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.349+4T>C
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3086
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
hgvs: c.818+4T>C
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

14-24800411-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800411
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800411
    reference: chr 14
allele count: 2
allele frequency: 1.648559982854976e-5
allele num: 121318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.818+3A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.818+3A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.422+3A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.25+3A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.818+3A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1277+3A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.349+3A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.818+3A>G
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2213
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3451
  bin: 7.75e1
  variant carriers: 0
hgvs: c.818+3A>G
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

14-24800424-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800424
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800424
    reference: chr 14
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.808C>G
  hgvsp: ENSP00000312126.4:p.Gln270Glu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.808C>G
  hgvsp: ENSP00000450477.1:p.Gln270Glu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.339C>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.808C>G
  hgvsp: ENSP00000452250.2:p.Gln270Glu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.412C>G
  hgvsp: ENSP00000450481.1:p.Gln138Glu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1267C>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.15C>G
  hgvsp: ENST00000396747.3:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.808C>G
  hgvsp: ENSP00000393177.2:p.Gln270Glu
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3085
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln270Glu
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

14-24800425-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800425
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800425
    reference: chr 14
allele count: 3
allele frequency: 2.471902705909495e-5
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.807C>T
  hgvsp: ENST00000554068.2:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.338C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.807C>T
  hgvsp: ENST00000418030.2:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.807C>T
  hgvsp: ENST00000310677.4:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1266C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.14C>T
  hgvsp: ENSP00000379971.3:p.Thr5Ile
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.807C>T
  hgvsp: ENST00000554781.1:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.411C>T
  hgvsp: ENST00000557056.1:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr5Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

14-24800429-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800429
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800429
    reference: chr 14
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.803G>C
  hgvsp: ENSP00000452250.2:p.Arg268Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.803G>C
  hgvsp: ENSP00000393177.2:p.Arg268Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1262G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.334G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.803G>C
  hgvsp: ENSP00000312126.4:p.Arg268Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.803G>C
  hgvsp: ENSP00000450477.1:p.Arg268Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.10G>C
  hgvsp: ENSP00000379971.3:p.Gly4Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.407G>C
  hgvsp: ENSP00000450481.1:p.Arg136Thr
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3447
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3085
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg268Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

14-24800431-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800431
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800431
    reference: chr 14
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.8G>C
  hgvsp: ENSP00000379971.3:p.Arg3Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.801G>C
  hgvsp: ENSP00000393177.2:p.Lys267Asn
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.801G>C
  hgvsp: ENSP00000452250.2:p.Lys267Asn
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.405G>C
  hgvsp: ENSP00000450481.1:p.Lys135Asn
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.801G>C
  hgvsp: ENSP00000312126.4:p.Lys267Asn
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1260G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.332G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.801G>C
  hgvsp: ENSP00000450477.1:p.Lys267Asn
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2214
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys267Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

14-24800431-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800431
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800431
    reference: chr 14
allele count: 13
allele frequency: 1.071087235935801e-4
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.332G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.405G>A
  hgvsp: ENST00000557056.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.801G>A
  hgvsp: ENST00000554781.1:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.8G>A
  hgvsp: ENSP00000379971.3:p.Arg3Lys
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.801G>A
  hgvsp: ENST00000554068.2:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.801G>A
  hgvsp: ENST00000418030.2:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.801G>A
  hgvsp: ENST00000310677.4:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1260G>A
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3085
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg3Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

14-24800437-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800437
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800437
    reference: chr 14
allele count: 13
allele frequency: 1.070981348447901e-4
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.795T>A
  hgvsp: ENSP00000393177.2:p.Tyr265Ter
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.795T>A
  hgvsp: ENSP00000312126.4:p.Tyr265Ter
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1254T>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.2T>A
  hgvsp: ENSP00000379971.3:p.Met1?
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.399T>A
  hgvsp: ENSP00000450481.1:p.Tyr133Ter
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.326T>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.795T>A
  hgvsp: ENSP00000450477.1:p.Tyr265Ter
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.795T>A
  hgvsp: ENSP00000452250.2:p.Tyr265Ter
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3447
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr265Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ

14-24800439-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800439
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800439
    reference: chr 14
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.793T>C
  hgvsp: ENSP00000312126.4:p.Tyr265His
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.397T>C
  hgvsp: ENSP00000450481.1:p.Tyr133His
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.793T>C
  hgvsp: ENSP00000450477.1:p.Tyr265His
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.793T>C
  hgvsp: ENSP00000452250.2:p.Tyr265His
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-1T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1252T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.793T>C
  hgvsp: ENSP00000393177.2:p.Tyr265His
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.324T>C
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2377
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr265His
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

14-24800443-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800443
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800443
    reference: chr 14
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.789C>T
  hgvsp: ENST00000418030.2:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-5C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.320C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.393C>T
  hgvsp: ENST00000557056.1:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.789C>T
  hgvsp: ENST00000310677.4:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.789C>T
  hgvsp: ENST00000554068.2:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.789C>T
  hgvsp: ENST00000554781.1:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1248C>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3449
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser263Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

14-24800447-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800447
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800447
    reference: chr 14
allele count: 2
allele frequency: 1.650818806127839e-5
allele num: 121152
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-9A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.785A>C
  hgvsp: ENSP00000393177.2:p.His262Pro
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.785A>C
  hgvsp: ENSP00000312126.4:p.His262Pro
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.785A>C
  hgvsp: ENSP00000450477.1:p.His262Pro
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.785A>C
  hgvsp: ENSP00000452250.2:p.His262Pro
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1244A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.316A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.389A>C
  hgvsp: ENSP00000450481.1:p.His130Pro
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 8043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3416
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39015
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His262Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

14-24800471-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800471
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800471
    reference: chr 14
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.365G>A
  hgvsp: ENSP00000450481.1:p.Arg122Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.761G>A
  hgvsp: ENSP00000312126.4:p.Arg254Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.761G>A
  hgvsp: ENSP00000450477.1:p.Arg254Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.761G>A
  hgvsp: ENSP00000452250.2:p.Arg254Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.761G>A
  hgvsp: ENSP00000393177.2:p.Arg254Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.292G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-33G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1220G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg254Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

14-24800472-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800472
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800472
    reference: chr 14
allele count: 9
allele frequency: 7.413753336189001e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.760C>T
  hgvsp: ENSP00000452250.2:p.Arg254Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.760C>T
  hgvsp: ENSP00000450477.1:p.Arg254Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1219C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.760C>T
  hgvsp: ENSP00000393177.2:p.Arg254Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-34C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.291C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.364C>T
  hgvsp: ENSP00000450481.1:p.Arg122Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.760C>T
  hgvsp: ENSP00000312126.4:p.Arg254Trp
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8423
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39095
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg254Trp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

14-24800472-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800472
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800472
    reference: chr 14
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.760C>A
  hgvsp: ENST00000310677.4:c.760C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-34C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.291C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.760C>A
  hgvsp: ENST00000418030.2:c.760C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.760C>A
  hgvsp: ENST00000554781.1:c.760C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1219C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.364C>A
  hgvsp: ENST00000557056.1:c.364C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.760C>A
  hgvsp: ENST00000554068.2:c.760C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2214
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg254Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

14-24800477-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800477
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800477
    reference: chr 14
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.359G>A
  hgvsp: ENSP00000450481.1:p.Gly120Glu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.286G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.755G>A
  hgvsp: ENSP00000450477.1:p.Gly252Glu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1214G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.755G>A
  hgvsp: ENSP00000312126.4:p.Gly252Glu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.755G>A
  hgvsp: ENSP00000393177.2:p.Gly252Glu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-39G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.755G>A
  hgvsp: ENSP00000452250.2:p.Gly252Glu
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2361
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly252Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-24800478-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800478
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800478
    reference: chr 14
allele count: 6
allele frequency: 4.942502224126001e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.754G>A
  hgvsp: ENSP00000393177.2:p.Gly252Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.754G>A
  hgvsp: ENSP00000452250.2:p.Gly252Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.358G>A
  hgvsp: ENSP00000450481.1:p.Gly120Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-40G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.754G>A
  hgvsp: ENSP00000312126.4:p.Gly252Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.285G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1213G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.754G>A
  hgvsp: ENSP00000450477.1:p.Gly252Arg
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3073
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39098
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3444
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly252Arg
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

14-24800484-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800484
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800484
    reference: chr 14
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.352G>A
  hgvsp: ENSP00000450481.1:p.Gly118Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.748G>A
  hgvsp: ENSP00000452250.2:p.Gly250Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.748G>A
  hgvsp: ENSP00000450477.1:p.Gly250Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.748G>A
  hgvsp: ENSP00000393177.2:p.Gly250Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.748G>A
  hgvsp: ENSP00000312126.4:p.Gly250Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-46G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1207G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.279G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8431
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3443
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly250Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

14-24800491-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800491
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800491
    reference: chr 14
allele count: 35
allele frequency: 2.883268803031551e-4
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1200G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.345G>A
  hgvsp: ENST00000557056.1:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.741G>A
  hgvsp: ENST00000418030.2:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-53G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.741G>A
  hgvsp: ENST00000310677.4:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.741G>A
  hgvsp: ENST00000554068.2:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.741G>A
  hgvsp: ENST00000554781.1:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.272G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8424
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3065
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3442
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu247Leu
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

14-24800495-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800495
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800495
    reference: chr 14
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.268G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-57G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.737G>A
  hgvsp: ENSP00000393177.2:p.Arg246Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.737G>A
  hgvsp: ENSP00000452250.2:p.Arg246Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.341G>A
  hgvsp: ENSP00000450481.1:p.Arg114Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.737G>A
  hgvsp: ENSP00000312126.4:p.Arg246Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.737G>A
  hgvsp: ENSP00000450477.1:p.Arg246Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1196G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg246Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

14-24800496-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800496
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800496
    reference: chr 14
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1195C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.736C>T
  hgvsp: ENSP00000312126.4:p.Arg246Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-58C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.736C>T
  hgvsp: ENSP00000452250.2:p.Arg246Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.267C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.736C>T
  hgvsp: ENSP00000393177.2:p.Arg246Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.340C>T
  hgvsp: ENSP00000450481.1:p.Arg114Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.736C>T
  hgvsp: ENSP00000450477.1:p.Arg246Trp
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg246Trp
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

14-24800498-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800498
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800498
    reference: chr 14
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.734C>T
  hgvsp: ENSP00000450477.1:p.Ala245Val
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.338C>T
  hgvsp: ENSP00000450481.1:p.Ala113Val
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.734C>T
  hgvsp: ENSP00000452250.2:p.Ala245Val
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.265C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.734C>T
  hgvsp: ENSP00000393177.2:p.Ala245Val
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.734C>T
  hgvsp: ENSP00000312126.4:p.Ala245Val
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-60C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1193C>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2363
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala245Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-24800499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800499
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800499
    reference: chr 14
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.733G>A
  hgvsp: ENSP00000393177.2:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.733G>A
  hgvsp: ENSP00000312126.4:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1192G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.337G>A
  hgvsp: ENSP00000450481.1:p.Ala113Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.733G>A
  hgvsp: ENSP00000450477.1:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.733G>A
  hgvsp: ENSP00000452250.2:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-61G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.264G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala245Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

14-24800500-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800500
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800500
    reference: chr 14
allele count: 21
allele frequency: 1.729989784822223e-4
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.732G>A
  hgvsp: ENSP00000450477.1:p.Met244Ile
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.263G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.732G>A
  hgvsp: ENSP00000312126.4:p.Met244Ile
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.732G>A
  hgvsp: ENSP00000452250.2:p.Met244Ile
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.732G>A
  hgvsp: ENSP00000393177.2:p.Met244Ile
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-62G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.336G>A
  hgvsp: ENSP00000450481.1:p.Met112Ile
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1191G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 20916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8426
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39163
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Met244Ile
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP

14-24800501-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800501
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800501
    reference: chr 14
allele count: 69
allele frequency: 5.684345805941377e-4
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.731T>A
  hgvsp: ENSP00000312126.4:p.Met244Lys
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.731T>A
  hgvsp: ENSP00000393177.2:p.Met244Lys
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.731T>A
  hgvsp: ENSP00000450477.1:p.Met244Lys
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.731T>A
  hgvsp: ENSP00000452250.2:p.Met244Lys
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-63T>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.262T>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.335T>A
  hgvsp: ENSP00000450481.1:p.Met112Lys
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1190T>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2200
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Met244Lys
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

14-24800504-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800504
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800504
    reference: chr 14
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.332T>C
  hgvsp: ENSP00000450481.1:p.Ile111Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1187T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.728T>C
  hgvsp: ENSP00000452250.2:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-66T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.728T>C
  hgvsp: ENSP00000312126.4:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.728T>C
  hgvsp: ENSP00000393177.2:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.728T>C
  hgvsp: ENSP00000450477.1:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.259T>C
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3439
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8427
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile243Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

14-24800522-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800522
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800522
    reference: chr 14
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.710G>A
  hgvsp: ENSP00000452250.2:p.Arg237Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.710G>A
  hgvsp: ENSP00000450477.1:p.Arg237Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.710G>A
  hgvsp: ENSP00000312126.4:p.Arg237Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1169G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.314G>A
  hgvsp: ENSP00000450481.1:p.Arg105Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.710G>A
  hgvsp: ENSP00000393177.2:p.Arg237Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-84G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.241G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3435
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg237Gln
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

14-24800523-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800523
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800523
    reference: chr 14
allele count: 5
allele frequency: 4.120652711389484e-5
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.709C>T
  hgvsp: ENSP00000452250.2:p.Arg237Ter
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1168C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.313C>T
  hgvsp: ENSP00000450481.1:p.Arg105Ter
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.709C>T
  hgvsp: ENSP00000393177.2:p.Arg237Ter
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.709C>T
  hgvsp: ENSP00000312126.4:p.Arg237Ter
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.709C>T
  hgvsp: ENSP00000450477.1:p.Arg237Ter
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.240C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-85C>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2361
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg237Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

14-24800523-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800523
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800523
    reference: chr 14
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.709C>G
  hgvsp: ENSP00000450477.1:p.Arg237Gly
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.709C>G
  hgvsp: ENSP00000452250.2:p.Arg237Gly
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-85C>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.709C>G
  hgvsp: ENSP00000312126.4:p.Arg237Gly
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1168C>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.709C>G
  hgvsp: ENSP00000393177.2:p.Arg237Gly
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.313C>G
  hgvsp: ENSP00000450481.1:p.Arg105Gly
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.240C>G
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8413
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39098
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg237Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

14-24800544-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800544
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800544
    reference: chr 14
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.292A>G
  hgvsp: ENSP00000450481.1:p.Ile98Val
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-106A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.688A>G
  hgvsp: ENSP00000452250.2:p.Ile230Val
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.688A>G
  hgvsp: ENSP00000450477.1:p.Ile230Val
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.688A>G
  hgvsp: ENSP00000312126.4:p.Ile230Val
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.688A>G
  hgvsp: ENSP00000393177.2:p.Ile230Val
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.219A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1147A>G
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8372
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile230Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

14-24800577-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800577
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800577
    reference: chr 14
allele count: 64
allele frequency: 5.311820460468436e-4
allele num: 120486
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.201-15G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-124-15G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.670-15G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.670-15G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.670-15G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.670-15G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1114G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.274-15G>A
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25850
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20035
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8020
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-24800579-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800579
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800579
    reference: chr 14
allele count: 2
allele frequency: 1.660191918185742e-5
allele num: 120468
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.670-17A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.201-17A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1112A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.670-17A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-124-17A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.274-17A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.670-17A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.670-17A>G
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP

14-24800581-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800581
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800581
    reference: chr 14
allele count: 2
allele frequency: 1.661295145695584e-5
allele num: 120388
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.670-19T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1110T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.274-19T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.670-19T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.670-19T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.201-19T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-124-19T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.670-19T>C
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3361
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

14-24800590-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800590
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800590
    reference: chr 14
allele count: 1
allele frequency: 8.320159747067144e-6
allele num: 120190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.670-28A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1101A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.201-28A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.274-28A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.670-28A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.670-28A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.670-28A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-124-28A>C
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7810
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34908
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

14-24800599-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800599
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800599
    reference: chr 14
allele count: 1
allele frequency: 8.344598541364175e-6
allele num: 119838
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.670-37G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-124-37G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.670-37G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.670-37G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.274-37G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1092G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.201-37G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.670-37G>A
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7482
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2226
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2339
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1205
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30791
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

14-24800609-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800609
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800609
    reference: chr 14
allele count: 1
allele frequency: 8.387432271484408e-6
allele num: 119226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.670-47T>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-124-47T>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.274-47T>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.670-47T>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.670-47T>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1082T>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.670-47T>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.201-47T>A
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2127
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2341
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4384
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3074
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

14-24800613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800613
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800613
    reference: chr 14
allele count: 9
allele frequency: 7.575502508333052e-5
allele num: 118804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-124-51C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.1078C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.670-51C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.670-51C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.274-51C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.670-51C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.201-51C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.670-51C>T
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7784
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14829
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2764
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2329
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17195
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

14-24800948-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800948
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800948
    reference: chr 14
allele count: 3
allele frequency: 3.713147015867515e-5
allele num: 80794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.273+46T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.743T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-125+46T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.200+46T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.669+46T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.669+46T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.669+46T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.669+46T>C
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20706
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10025
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2456
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4037
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

14-24800956-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800956
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800956
    reference: chr 14
allele count: 1
allele frequency: 1.221329294804465e-5
allele num: 81878
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.669+38G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.669+38G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.200+38G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.735G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.669+38G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.669+38G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-125+38G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.273+38G>A
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5198
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

14-24800964-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800964
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800964
    reference: chr 14
allele count: 2
allele frequency: 2.347417840375587e-5
allele num: 85200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.669+30C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-125+30C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.727C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.669+30C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.200+30C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.669+30C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.273+30C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.669+30C>T
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20710
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14083
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4388
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3665
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1504
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

14-24800968-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800968
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800968
    reference: chr 14
allele count: 61
allele frequency: 6.929298436932024e-4
allele num: 88032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.723G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.669+26G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.669+26G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.200+26G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.669+26G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.669+26G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.273+26G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-125+26G>C
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11188
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15090
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25051
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1217
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3722
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

14-24800980-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800980
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800980
    reference: chr 14
allele count: 1
allele frequency: 1.050508446087906e-5
allele num: 95192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.273+14A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.669+14A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.669+14A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.711A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-125+14A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.669+14A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.669+14A>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.200+14A>G
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33423
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2662
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

14-24800984-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800984
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800984
    reference: chr 14
allele count: 3
allele frequency: 3.077491229149997e-5
allele num: 97482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.669+10G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-125+10G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.669+10G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.669+10G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.707G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.669+10G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.273+10G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.200+10G>A
  variant of: http://identifiers.org/hgnc/235
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10911
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11554
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1216
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35455
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2050
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

14-24800986-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800986
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800986
    reference: chr 14
allele count: 1
allele frequency: 1.011326860841424e-5
allele num: 98880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.669+8G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.669+8G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.705G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.669+8G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.200+8G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-125+8G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.273+8G>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.669+8G>C
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2482
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36770
  bin: 6.25e1
  variant carriers: 0
hgvs: c.669+8G>C
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

14-24800986-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800986
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800986
    reference: chr 14
allele count: 2
allele frequency: 2.022653721682848e-5
allele num: 98880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.669+8G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.200+8G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.273+8G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-125+8G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.705G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.669+8G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.669+8G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.669+8G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 7.25e1
  variant carriers: 0
hgvs: c.669+8G>A
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

14-24800987-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800987
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800987
    reference: chr 14
allele count: 1
allele frequency: 1.002124503948371e-5
allele num: 99788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.669+7C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.669+7C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.669+7C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.704C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.273+7C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.669+7C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-125+7C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.200+7C>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35317
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9894
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10600
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
hgvs: c.669+7C>A
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

14-24800987-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800987
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800987
    reference: chr 14
allele count: 1
allele frequency: 1.002124503948371e-5
allele num: 99788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.704C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.669+7C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.669+7C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-125+7C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.200+7C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.669+7C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.669+7C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.273+7C>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35317
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9894
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2557
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
hgvs: c.669+7C>T
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

14-24800988-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800988
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24800988
    reference: chr 14
allele count: 2
allele frequency: 1.991833482720844e-5
allele num: 100410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.669+6C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.669+6C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.669+6C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-125+6C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.669+6C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.703C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.200+6C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.273+6C>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 5.25e1
  variant carriers: 0
hgvs: c.669+6C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

14-24800990-T-TGACCTGGTGCTTCTTCTCGGTGTCCAGCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24800990
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801019
    reference: chr 14
allele count: 17
allele frequency: 1.660707656839185e-4
allele num: 102366
alternate allele: TGACCTGGTGCTTCTTCTCGGTGTCCAGCC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7189
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36808
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39959
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9606
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum

14-24801001-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801001
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801001
    reference: chr 14
allele count: 1
allele frequency: 9.321054397673465e-6
allele num: 107284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-132A>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.662A>T
  hgvsp: ENSP00000452250.2:p.Lys221Met
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.662A>T
  hgvsp: ENSP00000450477.1:p.Lys221Met
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.662A>T
  hgvsp: ENSP00000393177.2:p.Lys221Met
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.193A>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.662A>T
  hgvsp: ENSP00000312126.4:p.Lys221Met
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.266A>T
  hgvsp: ENSP00000450481.1:p.Lys89Met
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.690A>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys221Met
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

14-24801003-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801003
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801003
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 107694
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.660G>A
  hgvsp: ENST00000310677.4:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.660G>A
  hgvsp: ENST00000418030.2:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.264G>A
  hgvsp: ENST00000557056.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.660G>A
  hgvsp: ENST00000554781.1:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.660G>A
  hgvsp: ENST00000554068.2:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-134G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.688G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.191G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys220Lys
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

14-24801009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801009
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801009
    reference: chr 14
allele count: 50
allele frequency: 4.573142846689959e-4
allele num: 109334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.654C>T
  hgvsp: ENST00000554068.2:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.682C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.185C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.654C>T
  hgvsp: ENST00000310677.4:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.654C>T
  hgvsp: ENST00000418030.2:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-140C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.654C>T
  hgvsp: ENST00000554781.1:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.258C>T
  hgvsp: ENST00000557056.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9012
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39973
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 9.75e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr218Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

14-24801009-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801009
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801009
    reference: chr 14
allele count: 1
allele frequency: 9.146285693379919e-6
allele num: 109334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.654C>A
  hgvsp: ENST00000554781.1:c.654C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-140C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.654C>A
  hgvsp: ENST00000418030.2:c.654C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.654C>A
  hgvsp: ENST00000310677.4:c.654C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.682C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.258C>A
  hgvsp: ENST00000557056.1:c.258C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.185C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.654C>A
  hgvsp: ENST00000554068.2:c.654C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9012
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr218Thr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/14-24801022-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801022
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801022
    reference: chr 14
allele count: 1
allele frequency: 8.958004873154651e-6
allele num: 111632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.641G>T
  hgvsp: ENSP00000393177.2:p.Arg214Leu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.641G>T
  hgvsp: ENSP00000450477.1:p.Arg214Leu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.641G>T
  hgvsp: ENSP00000312126.4:p.Arg214Leu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.245G>T
  hgvsp: ENSP00000450481.1:p.Arg82Leu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.172G>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.669G>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.641G>T
  hgvsp: ENSP00000452250.2:p.Arg214Leu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-153G>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3475
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg214Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

14-24801023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801023
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801023
    reference: chr 14
allele count: 2
allele frequency: 1.789100797938956e-5
allele num: 111788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.640C>T
  hgvsp: ENSP00000452250.2:p.Arg214Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.640C>T
  hgvsp: ENSP00000312126.4:p.Arg214Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.640C>T
  hgvsp: ENSP00000393177.2:p.Arg214Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.640C>T
  hgvsp: ENSP00000450477.1:p.Arg214Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.668C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.244C>T
  hgvsp: ENSP00000450481.1:p.Arg82Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-154C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.171C>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg214Trp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/14-24801029-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801029
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801029
    reference: chr 14
allele count: 1
allele frequency: 8.902658333778466e-6
allele num: 112326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.634T>G
  hgvsp: ENSP00000393177.2:p.Ser212Ala
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-160T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.634T>G
  hgvsp: ENSP00000452250.2:p.Ser212Ala
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.634T>G
  hgvsp: ENSP00000312126.4:p.Ser212Ala
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.238T>G
  hgvsp: ENSP00000450481.1:p.Ser80Ala
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.662T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.634T>G
  hgvsp: ENSP00000450477.1:p.Ser212Ala
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.165T>G
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser212Ala
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-24801034-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801034
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801034
    reference: chr 14
allele count: 2
allele frequency: 1.778663156771371e-5
allele num: 112444
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.160T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.233T>G
  hgvsp: ENSP00000450481.1:p.Leu78Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.629T>G
  hgvsp: ENSP00000312126.4:p.Leu210Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.657T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.629T>G
  hgvsp: ENSP00000452250.2:p.Leu210Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.629T>G
  hgvsp: ENSP00000450477.1:p.Leu210Arg
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-165T>G
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.629T>G
  hgvsp: ENSP00000393177.2:p.Leu210Arg
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4040
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10917
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39813
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu210Arg
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

14-24801036-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801036
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801036
    reference: chr 14
allele count: 1
allele frequency: 8.890311338703082e-6
allele num: 112482
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.627C>T
  hgvsp: ENST00000310677.4:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.627C>T
  hgvsp: ENST00000554781.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.158C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.627C>T
  hgvsp: ENST00000418030.2:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-167C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.231C>T
  hgvsp: ENST00000557056.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.655C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.627C>T
  hgvsp: ENST00000554068.2:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3553
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45915
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser209Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-24801037-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801037
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801037
    reference: chr 14
allele count: 1
allele frequency: 8.887940841865756e-6
allele num: 112512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.157C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.230C>A
  hgvsp: ENSP00000450481.1:p.Ser77Tyr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.626C>A
  hgvsp: ENSP00000393177.2:p.Ser209Tyr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.626C>A
  hgvsp: ENSP00000452250.2:p.Ser209Tyr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.626C>A
  hgvsp: ENSP00000450477.1:p.Ser209Tyr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.626C>A
  hgvsp: ENSP00000312126.4:p.Ser209Tyr
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.654C>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-168C>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10953
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5145
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser209Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-24801045-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801045
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801045
    reference: chr 14
allele count: 1206
allele frequency: 1.072476656291685e-2
allele num: 112450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.618A>T
  hgvsp: ENST00000554068.2:c.618A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.618A>T
  hgvsp: ENST00000554781.1:c.618A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.646A>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.618A>T
  hgvsp: ENST00000418030.2:c.618A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.618A>T
  hgvsp: ENST00000310677.4:c.618A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-176A>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.222A>T
  hgvsp: ENST00000557056.1:c.222A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.149A>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 7.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 1.75e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 38391
  bin: 2.25e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 1.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10983
  bin: 2.75e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 3.25e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 7.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala206Ala
num of homozygotes: 64
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

14-24801052-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801052
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801052
    reference: chr 14
allele count: 2
allele frequency: 1.790959237767748e-5
allele num: 111672
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.611G>A
  hgvsp: ENSP00000312126.4:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.215G>A
  hgvsp: ENSP00000450481.1:p.Arg72Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.611G>A
  hgvsp: ENSP00000393177.2:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.611G>A
  hgvsp: ENSP00000450477.1:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.142G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-183G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.611G>A
  hgvsp: ENSP00000452250.2:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.639G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11410
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5759
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg204Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

14-24801053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801053
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801053
    reference: chr 14
allele count: 5
allele frequency: 4.473872584108804e-5
allele num: 111760
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.610C>T
  hgvsp: ENSP00000312126.4:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.610C>T
  hgvsp: ENSP00000452250.2:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.610C>T
  hgvsp: ENSP00000393177.2:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-184C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.141C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.610C>T
  hgvsp: ENSP00000450477.1:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.638C>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.214C>T
  hgvsp: ENSP00000450481.1:p.Arg72Trp
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37159
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg204Trp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/14-24801057-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801057
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801057
    reference: chr 14
allele count: 1
allele frequency: 8.984403076259613e-6
allele num: 111304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.606G>T
  hgvsp: ENST00000554781.1:c.606G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.606G>T
  hgvsp: ENST00000310677.4:c.606G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.210G>T
  hgvsp: ENST00000557056.1:c.210G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.634G>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-188G>T
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.606G>T
  hgvsp: ENST00000418030.2:c.606G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.606G>T
  hgvsp: ENST00000554068.2:c.606G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.137G>T
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr202Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

14-24801080-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801080
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801080
    reference: chr 14
allele count: 1
allele frequency: 9.19777046044039e-6
allele num: 108722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.583A>C
  hgvsp: ENSP00000393177.2:p.Met195Leu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.583A>C
  hgvsp: ENSP00000450477.1:p.Met195Leu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.583A>C
  hgvsp: ENSP00000312126.4:p.Met195Leu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-211A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.187A>C
  hgvsp: ENSP00000450481.1:p.Met63Leu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.583A>C
  hgvsp: ENSP00000452250.2:p.Met195Leu
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.611A>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.114A>C
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10902
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1779
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8922
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Met195Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

14-24801082-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801082
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801082
    reference: chr 14
allele count: 3
allele frequency: 2.768242719521648e-5
allele num: 108372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.609T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.581T>C
  hgvsp: ENSP00000312126.4:p.Leu194Pro
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.581T>C
  hgvsp: ENSP00000452250.2:p.Leu194Pro
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.185T>C
  hgvsp: ENSP00000450481.1:p.Leu62Pro
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.112T>C
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.581T>C
  hgvsp: ENSP00000450477.1:p.Leu194Pro
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.581T>C
  hgvsp: ENSP00000393177.2:p.Leu194Pro
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-213T>C
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5936
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10748
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1847
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu194Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

14-24801084-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24801084
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24801084
    reference: chr 14
allele count: 5
allele frequency: 4.629200999907416e-5
allele num: 108010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000379971
  ensembl transcript: ENST00000396747
  gene symbol: ADCY4
  hgvsc: ENST00000396747.3:c.-215G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000452250
  ensembl transcript: ENST00000554068
  gene symbol: ADCY4
  hgvsc: ENST00000554068.2:c.579G>A
  hgvsp: ENST00000554068.2:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554577
  gene symbol: ADCY4
  hgvsc: ENST00000554577.1:n.607G>A
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450477
  ensembl transcript: ENST00000554781
  gene symbol: ADCY4
  hgvsc: ENST00000554781.1:c.579G>A
  hgvsp: ENST00000554781.1:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000450481
  ensembl transcript: ENST00000557056
  gene symbol: ADCY4
  hgvsc: ENST00000557056.1:c.183G>A
  hgvsp: ENST00000557056.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000393177
  ensembl transcript: ENST00000418030
  gene symbol: ADCY4
  hgvsc: ENST00000418030.2:c.579G>A
  hgvsp: ENST00000418030.2:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129467
  ensembl protein: ENSP00000312126
  ensembl transcript: ENST00000310677
  gene symbol: ADCY4
  hgvsc: ENST00000310677.4:c.579G>A
  hgvsp: ENST00000310677.4:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/235
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129467
  ensembl transcript: ENST00000554674
  gene symbol: ADCY4
  hgvsc: ENST00000554674.1:n.110G>A
  variant of: http://identifiers.org/hgnc/235
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31098
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala193Ala
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 337
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8334
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
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: 1.50195253829979e-5
allele num: 66580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

DP
type: SiteQuality
SIO_000300: 1.596648e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.929999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.344e0

QD
type: SiteQuality
SIO_000300: 1.197e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.77e-1

QD
type: SiteQuality
SIO_000300: 1.308e1

VQSLOD
type: SiteQuality
SIO_000300: -1.342e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

FS
type: SiteQuality
SIO_000300: 5.708e0

MQ
type: SiteQuality
SIO_000300: 5.866e1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.815e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.44e-1

DP
type: SiteQuality
SIO_000300: 1.600274e6

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.0960741282614e-5
allele num: 16404
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: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502178158329578e-5
allele num: 66570
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.05e0

FS
type: SiteQuality
SIO_000300: 4.4854e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 4.93e0

VQSLOD
type: SiteQuality
SIO_000300: -1.035e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

DP
type: SiteQuality
SIO_000300: 1.602348e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3086
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

QD
type: SiteQuality
SIO_000300: 1.097e1

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

FS
type: SiteQuality
SIO_000300: 4.018e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.385e0

VQSLOD
type: SiteQuality
SIO_000300: 7.08e-1

DP
type: SiteQuality
SIO_000300: 1.603135e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.56e0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 2214
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500990217847926e-5
allele num: 66652
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.676e0

DP
type: SiteQuality
SIO_000300: 1.606006e6

MQRankSum
type: SiteQuality
SIO_000300: 6.27e-1

MQ
type: SiteQuality
SIO_000300: 5.881e1

QD
type: SiteQuality
SIO_000300: 1.319e1

FS
type: SiteQuality
SIO_000300: 6.298e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.029e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.49e-1

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
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variant carriers: 3

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

GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 3086
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000120004800192e-5
allele num: 66664
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.148e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.429e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

DP
type: SiteQuality
SIO_000300: 1.606435e6

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.97e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.429e1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.148e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.606435e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000120004800192e-5
allele num: 66664
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.17e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.7023e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.267e0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.986e1

BaseQRankSum
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.607882e6

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3085
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497885993583016e-5
allele num: 66698
num of homozygotes: 0

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.143e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

BaseQRankSum
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SIO_000300: -2.849e0

MQ
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SIO_000300: 5.786e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.051e0

DP
type: SiteQuality
SIO_000300: 1.607903e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-1

MQ
type: SiteQuality
SIO_000300: 5.921e1

QD
type: SiteQuality
SIO_000300: 1.283e1

DP
type: SiteQuality
SIO_000300: 1.608105e6

InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.317e0

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-1

FS
type: SiteQuality
SIO_000300: 3.622e0

VQSLOD
type: SiteQuality
SIO_000300: 6.47e-1

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -3.573e0

DP
type: SiteQuality
SIO_000300: 1.609002e6

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.45e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 13

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.994423457456377e-5
allele num: 66708
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.058361052313275e-3
allele num: 6614
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.45e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.573e0

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

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

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.058361052313275e-3
allele num: 6614
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.993344924755681e-5
allele num: 66716
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

QD
type: SiteQuality
SIO_000300: 1.842e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 1.113e0

DP
type: SiteQuality
SIO_000300: 1.609057e6

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

FS
type: SiteQuality
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InbreedingCoeff
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.25e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
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QD
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
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DP
type: SiteQuality
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InbreedingCoeff
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FS
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MQ
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 1
allele frequency: 9.665571235260003e-5
allele num: 10346
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502133028901039e-5
allele num: 66572
num of homozygotes: 0

Other
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num of homozygotes: 0

Latino
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East Asian
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South Asian
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European (Finnish)
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FS
type: SiteQuality
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BaseQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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Latino
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allele num: 11576
num of homozygotes: 0

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

South Asian
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Other
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 2.26e0

MQ
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DP
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ClippingRankSum
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SIO_000300: 9.28e-1

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
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allele frequency: 5.767012687427913e-4
allele num: 10404
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -3.45e-1

InbreedingCoeff
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MQRankSum
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DP
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FS
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ReadPosRankSum
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QD
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VQSLOD
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ClippingRankSum
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SIO_000300: -4.18e-1

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

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

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

QD
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 4.024e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.18e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

VQSLOD
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.608999e6

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.87e-1

BaseQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.841e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.994485073732166e-5
allele num: 66728
num of homozygotes: 0

European (Finnish)
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allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.281e0

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.609243e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.06e-1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
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allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

South Asian
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allele frequency: 2.119927316777711e-3
allele num: 16510
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East Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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QD
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FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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num of homozygotes: 0

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

South Asian
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European (Non-Finnish)
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allele num: 66718
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Other
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European (Finnish)
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African
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Latino
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QD
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FS
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

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

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

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

MQ
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SIO_000300: 5.891e1

MQRankSum
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QD
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FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
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SIO_000300: 7.85e-1

VQSLOD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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DP
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InbreedingCoeff
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SIO_000300: 0.0e0

QD
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MQ
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SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66720
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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East Asian
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allele count: 21
allele frequency: 2.427184466019417e-3
allele num: 8652
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11576
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
type: SiteQuality
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BaseQRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 8
allele frequency: 1.199076710932582e-4
allele num: 66718
num of homozygotes: 0

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

Latino
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allele frequency: 5.010366275051832e-3
allele num: 11576
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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QD
type: SiteQuality
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MQRankSum
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FS
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DP
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.954e1

ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

European (Finnish)
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allele count: 0
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FS
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MQ
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ReadPosRankSum
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VQSLOD
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QD
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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African
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Latino
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European (Non-Finnish)
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allele num: 66688
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FS
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ReadPosRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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Latino
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South Asian
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Other
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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African
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Other
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South Asian
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MQ
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DP
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.288e0

QD
type: SiteQuality
SIO_000300: 1.308e1

GenotypeQuality
all individuals: 37164
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 137
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 9.75e1
variant carriers: 64

GenotypeQuality
all individuals: 426
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3369
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2960
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 63
allele frequency: 6.122448979591836e-3
allele num: 10290
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
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: 8594
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66202
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.582683e6

QD
type: SiteQuality
SIO_000300: 1.327e1

VQSLOD
type: SiteQuality
SIO_000300: 3.5e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.919e0

FS
type: SiteQuality
SIO_000300: 1.452e0

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.72e-1

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2970
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 457
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3373
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8031
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66178
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.218026796589525e-4
allele num: 16420
num of homozygotes: 1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.65e-2

QD
type: SiteQuality
SIO_000300: 2.73e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.579633e6

GenotypeQuality
all individuals: 36963
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 297
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8022
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2953
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2342
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.328288707799767e-4
allele num: 8590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66138
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

DP
type: SiteQuality
SIO_000300: 1.576156e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

QD
type: SiteQuality
SIO_000300: 1.326e1

FS
type: SiteQuality
SIO_000300: 3.544e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-1

GenotypeQuality
all individuals: 877
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3333
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2916
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66032
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.109481915933529e-5
allele num: 16368
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: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: -1.102e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.71e-1

QD
type: SiteQuality
SIO_000300: 1.352e1

DP
type: SiteQuality
SIO_000300: 1.553439e6

GenotypeQuality
all individuals: 1079
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3276
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2149
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7106
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2819
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2135
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518556763651825e-5
allele num: 65852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
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: 6530
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.51418e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.23e-1

FS
type: SiteQuality
SIO_000300: 2.927e0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.467e0

MQRankSum
type: SiteQuality
SIO_000300: -7.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

GenotypeQuality
all individuals: 3706
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2939
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2238
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20705
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6468
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2754
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16164
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525599560627327e-5
allele num: 65548
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.946e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 6.149e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: -1.828e0

DP
type: SiteQuality
SIO_000300: 1.472008e6

QD
type: SiteQuality
SIO_000300: 1.321e1

GenotypeQuality
all individuals: 454
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2136
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3769
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2352
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 176
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variant carriers: 0

GenotypeQuality
all individuals: 6376
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variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2960
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4832
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5007
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 8
allele frequency: 7.886435331230284e-4
allele num: 10144
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.221226825930074e-5
allele num: 16074
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-2

DP
type: SiteQuality
SIO_000300: 1.472323e6

VQSLOD
type: SiteQuality
SIO_000300: 3.14e0

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

QD
type: SiteQuality
SIO_000300: 1.481e1

GenotypeQuality
all individuals: 7202
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5335
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8793
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6654
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1872
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2654
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2948
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14026
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8012
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 4.392386530014642e-4
allele num: 6830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47102
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.26e0

DP
type: SiteQuality
SIO_000300: 7.92588e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

QD
type: SiteQuality
SIO_000300: 1.192e1

FS
type: SiteQuality
SIO_000300: 7.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.69e-1

GenotypeQuality
all individuals: 6037
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16089
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1194
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12700
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8220
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47634
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.449275362318841e-4
allele num: 6900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6686
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.46531e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.112e0

QD
type: SiteQuality
SIO_000300: 6.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.486e0

GenotypeQuality
all individuals: 378
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6109
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21139
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16298
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.03893533664526e-5
allele num: 49518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6934
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

MQ
type: SiteQuality
SIO_000300: 5.871e1

FS
type: SiteQuality
SIO_000300: 2.422e0

VQSLOD
type: SiteQuality
SIO_000300: -2.097e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.53e-1

QD
type: SiteQuality
SIO_000300: 1.04e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

DP
type: SiteQuality
SIO_000300: 9.40613e5

GenotypeQuality
all individuals: 529
bin: 9.75e1
variant carriers: 59

GenotypeQuality
all individuals: 2619
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1802
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15486
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25502
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51152
num of homozygotes: 0

African
type: Population
allele count: 60
allele frequency: 8.169934640522876e-3
allele num: 7344
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.142857142857143e-4
allele num: 8750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.347e1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

DP
type: SiteQuality
SIO_000300: 9.9509e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e-1

GenotypeQuality
all individuals: 12653
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 7.5e0
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GenotypeQuality
all individuals: 479
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2401
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
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variant carriers: 1

GenotypeQuality
all individuals: 580
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variant carriers: 0

GenotypeQuality
all individuals: 2274
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.295336787564767e-4
allele num: 7720
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7698
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4562
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.353e1

MQRankSum
type: SiteQuality
SIO_000300: -5.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.93e-1

MQ
type: SiteQuality
SIO_000300: 5.835e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.19e-1

DP
type: SiteQuality
SIO_000300: 1.099825e6

VQSLOD
type: SiteQuality
SIO_000300: -1.972e0

GenotypeQuality
all individuals: 114
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 622
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2213
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 473
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variant carriers: 0

GenotypeQuality
all individuals: 99
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variant carriers: 0

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

GenotypeQuality
all individuals: 680
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variant carriers: 0

GenotypeQuality
all individuals: 520
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variant carriers: 0

GenotypeQuality
all individuals: 236
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variant carriers: 0

GenotypeQuality
all individuals: 2367
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.680542110358181e-5
allele num: 10330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.775063902300483e-5
allele num: 56336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7844
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 684
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.154243860404998e-4
allele num: 4642
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.956e0

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

QD
type: SiteQuality
SIO_000300: 4.27e0

DP
type: SiteQuality
SIO_000300: 1.132273e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.174e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.369e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

FS
type: SiteQuality
SIO_000300: 4.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

GenotypeQuality
all individuals: 2009
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1114
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1856
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 7.5e0
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GenotypeQuality
all individuals: 10964
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variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
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variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 9.40379913485048e-5
allele num: 10634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57040
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7952
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4730
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.024e0

FS
type: SiteQuality
SIO_000300: 9.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.77e-1

QD
type: SiteQuality
SIO_000300: 9.35e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.151296e6

GenotypeQuality
all individuals: 724
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10964
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2009
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2482
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36770
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 473
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7952
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.524614996213078e-4
allele num: 7922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4730
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

DP
type: SiteQuality
SIO_000300: 1.151296e6

FS
type: SiteQuality
SIO_000300: 9.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

QD
type: SiteQuality
SIO_000300: 9.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.024e0

GenotypeQuality
all individuals: 646
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2557
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 37319
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
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variant carriers: 1

GenotypeQuality
all individuals: 160
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

African
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: 10870
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57480
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.226e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e-1

DP
type: SiteQuality
SIO_000300: 1.1618e6

VQSLOD
type: SiteQuality
SIO_000300: 5.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.73e-1

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

GenotypeQuality
all individuals: 160
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10600
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
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variant carriers: 0

GenotypeQuality
all individuals: 37319
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 605
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.73973556019485e-5
allele num: 57480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10870
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e-1

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

DP
type: SiteQuality
SIO_000300: 1.1618e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.35e-1

FS
type: SiteQuality
SIO_000300: 5.226e0

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

GenotypeQuality
all individuals: 665
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 658
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GenotypeQuality
all individuals: 489
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
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GenotypeQuality
all individuals: 37940
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GenotypeQuality
all individuals: 1702
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10314
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GenotypeQuality
all individuals: 549
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2592
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.459010722933241e-5
allele num: 57820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7994
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10974
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.17167e6

VQSLOD
type: SiteQuality
SIO_000300: -1.431e0

FS
type: SiteQuality
SIO_000300: 7.275e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -6.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 6.2e0

GenotypeQuality
all individuals: 116
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.722755428493635e-4
allele num: 58764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4930
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.21713729308666e-4
allele num: 8216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.7e-1

QD
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SIO_000300: 1.99e0

MQ
type: SiteQuality
SIO_000300: 4.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.49e-1

FS
type: SiteQuality
SIO_000300: 9.391e0

DP
type: SiteQuality
SIO_000300: 1.189846e6

MQRankSum
type: SiteQuality
SIO_000300: -3.26e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

Latino
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allele count: 1
allele frequency: 9.359790340696369e-5
allele num: 10684
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12760
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60962
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5190
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
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SIO_000300: -1.9e-3

DP
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SIO_000300: 1.247511e6

BaseQRankSum
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SIO_000300: 1.84e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.062e0

FS
type: SiteQuality
SIO_000300: 1.271e0

MQRankSum
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SIO_000300: 1.94e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.63e0

MQ
type: SiteQuality
SIO_000300: 5.859e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61122
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5206
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-2

QD
type: SiteQuality
SIO_000300: 9.5e0

BaseQRankSum
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SIO_000300: -1.652e0

DP
type: SiteQuality
SIO_000300: 1.252621e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

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

African
type: Population
allele count: 1
allele frequency: 1.141291942478886e-4
allele num: 8762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.887504718761797e-4
allele num: 5298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 46
allele frequency: 7.455671172485332e-4
allele num: 61698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13604
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.242144177449168e-5
allele num: 10820
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.278772378516624e-3
allele num: 782
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

DP
type: SiteQuality
SIO_000300: 1.272287e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

QD
type: SiteQuality
SIO_000300: 1.05e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61698
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.242144177449168e-5
allele num: 10820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5298
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13604
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.272287e6

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.05e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14532
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.102494083378845e-5
allele num: 10986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.168e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

DP
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.289e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.26e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5432
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.373042240151875e-4
allele num: 8428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14576
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62550
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.928e1

MQRankSum
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.870000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.939e-1

DP
type: SiteQuality
SIO_000300: 1.305319e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
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allele frequency: 0.0e0
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South Asian
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.594336915276936e-5
allele num: 62722
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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DP
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QD
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele num: 814
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5430
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.187352584942946e-5
allele num: 62748
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.81e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-2

FS
type: SiteQuality
SIO_000300: 6.271e0

MQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

DP
type: SiteQuality
SIO_000300: 1.311829e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 313
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14940
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9112
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.593422352528761e-5
allele num: 62758
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
SIO_000300: 9.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.08e-1

QD
type: SiteQuality
SIO_000300: 1.074e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.2e-2

DP
type: SiteQuality
SIO_000300: 1.311028e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.593523918794021e-5
allele num: 62754
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11010
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.842e-1

DP
type: SiteQuality
SIO_000300: 1.311465e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.65e0

MQ
type: SiteQuality
SIO_000300: 5.267e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.541e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-1

GenotypeQuality
all individuals: 5197
bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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variant carriers: 10

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1079

GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
all individuals: 579
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variant carriers: 14

GenotypeQuality
all individuals: 44683
bin: 6.25e1
variant carriers: 7

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5410
num of homozygotes: 0

African
type: Population
allele count: 1114
allele frequency: 1.203803760535984e-1
allele num: 9254
num of homozygotes: 63

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 3.194275857663068e-4
allele num: 62612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14964
num of homozygotes: 0

Latino
type: Population
allele count: 68
allele frequency: 6.193078324225865e-3
allele num: 10980
num of homozygotes: 1

Other
type: Population
allele count: 4
allele frequency: 4.938271604938272e-3
allele num: 810
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.480000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

DP
type: SiteQuality
SIO_000300: 1.318447e6

QD
type: SiteQuality
SIO_000300: 1.312e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 102
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14938
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.19047619047619e-4
allele num: 8400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.608337622233659e-5
allele num: 62176
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10930
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.13e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.856e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

DP
type: SiteQuality
SIO_000300: 1.299388e6

GenotypeQuality
all individuals: 139
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variant carriers: 0

GenotypeQuality
all individuals: 103
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 765
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GenotypeQuality
all individuals: 248
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9066
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.036776288295239e-5
allele num: 62214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10944
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14948
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.08e-1

FS
type: SiteQuality
SIO_000300: 4.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.65e-1

DP
type: SiteQuality
SIO_000300: 1.299546e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

QD
type: SiteQuality
SIO_000300: 1.2e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 244
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GenotypeQuality
all individuals: 487
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10900
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.1101243339254e-4
allele num: 9008
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61910
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14942
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.320000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.329e1

FS
type: SiteQuality
SIO_000300: 4.593e0

MQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

DP
type: SiteQuality
SIO_000300: 1.290345e6

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.657550140891762e-5
allele num: 60330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8250
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QD
type: SiteQuality
SIO_000300: 6.98e0

DP
type: SiteQuality
SIO_000300: 1.240302e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.01e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 196
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GenotypeQuality
all individuals: 489
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 466
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GenotypeQuality
all individuals: 675
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GenotypeQuality
all individuals: 2840
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14706
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.40379913485048e-5
allele num: 10634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8748
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.327012010513358e-5
allele num: 60114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5162
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.64e-1

FS
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.57e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.33e-1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.036e0