7-731197-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731197
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 731197
    reference: chr 7
allele count: 1
allele frequency: 6.252344629235963e-5
allele num: 15994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.178-10834C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.178-10834C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.178-10834C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.178-10834C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000394633
  ensembl transcript: ENST00000414568
  gene symbol: PRKAR1B
  hgvsc: ENST00000414568.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.178-10834C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.178-10834C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.178-10834C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.178-10834C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3002
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ

7-731205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731205
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 731205
    reference: chr 7
allele count: 12
allele frequency: 7.519739315703722e-4
allele num: 15958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.178-10842C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.178-10842C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000394633
  ensembl transcript: ENST00000414568
  gene symbol: PRKAR1B
  hgvsc: ENST00000414568.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.178-10842C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.178-10842C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.178-10842C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.178-10842C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.178-10842C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.178-10842C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5349
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

7-731212-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731212
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 731212
    reference: chr 7
allele count: 1
allele frequency: 6.298022420959819e-5
allele num: 15878
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.178-10849G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.178-10849G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000394633
  ensembl transcript: ENST00000414568
  gene symbol: PRKAR1B
  hgvsc: ENST00000414568.1:c.-24G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.178-10849G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.178-10849G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.178-10849G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.178-10849G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.178-10849G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.178-10849G>C
  variant of: http://identifiers.org/hgnc/9390
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

7-731212-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731212
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 731212
    reference: chr 7
allele count: 5
allele frequency: 3.149011210479909e-4
allele num: 15878
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.178-10849G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.178-10849G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.178-10849G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.178-10849G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.178-10849G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.178-10849G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.178-10849G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000394633
  ensembl transcript: ENST00000414568
  gene symbol: PRKAR1B
  hgvsc: ENST00000414568.1:c.-24G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.178-10849G>A
  variant of: http://identifiers.org/hgnc/9390
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2776
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

7-731223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731223
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 731223
    reference: chr 7
allele count: 8
allele frequency: 5.061369100341643e-4
allele num: 15806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.178-10860G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000394633
  ensembl transcript: ENST00000414568
  gene symbol: PRKAR1B
  hgvsc: ENST00000414568.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.178-10860G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.178-10860G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.178-10860G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.178-10860G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.178-10860G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.178-10860G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.178-10860G>A
  variant of: http://identifiers.org/hgnc/9390
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2559
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

7-750917-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750917
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750917
    reference: chr 7
allele count: 1
allele frequency: 8.474863554696769e-6
allele num: 117996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+49C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+49C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+49C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+49C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+49C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+49C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+49C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+49C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+49C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12365
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

7-750920-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750920
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750920
    reference: chr 7
allele count: 283
allele frequency: 2.396761407906772e-3
allele num: 118076
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+46G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+46G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+46G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+46G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+46G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+46G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+46G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+46G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+46G>C
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 4.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 11924
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 3.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5752
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 5.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13252
  bin: 2.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6854
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

7-750927-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750927
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750927
    reference: chr 7
allele count: 7
allele frequency: 5.914859817822318e-5
allele num: 118346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+39T>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+39T>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+39T>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+39T>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+39T>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+39T>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+39T>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+39T>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+39T>A
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11977
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5523
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7869
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18253
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6958
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-750929-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750929
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750929
    reference: chr 7
allele count: 2
allele frequency: 1.689360408149475e-5
allele num: 118388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+37C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+37C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+37C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+37C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+37C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+37C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+37C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+37C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+37C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 3.75e1
  variant carriers: 0
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: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/7-750932-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750932
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750932
    reference: chr 7
allele count: 4
allele frequency: 3.378834977699689e-5
allele num: 118384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+34G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+34G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+34G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+34G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+34G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+34G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+34G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+34G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+34G>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7430
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12224
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6960
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

7-750941-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750941
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750941
    reference: chr 7
allele count: 1
allele frequency: 8.398421096833796e-6
allele num: 119070
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+25C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+25C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+25C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+25C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+25C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+25C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+25C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+25C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+25C>A
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

7-750946-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750946
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750946
    reference: chr 7
allele count: 1
allele frequency: 8.369601606963508e-6
allele num: 119480
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+20C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+20C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+20C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+20C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+20C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+20C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+20C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+20C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+20C>A
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3867
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-750947-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750947
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750947
    reference: chr 7
allele count: 1
allele frequency: 8.364980844193866e-6
allele num: 119546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+19C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9066
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2938
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3869
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7206
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-750949-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750949
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750949
    reference: chr 7
allele count: 1
allele frequency: 8.363861427543869e-6
allele num: 119562
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+17G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+17G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+17G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+17G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+17G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+17G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+17G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+17G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+17G>C
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

7-750949-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750949
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750949
    reference: chr 7
allele count: 2
allele frequency: 1.672772285508774e-5
allele num: 119562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+17G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+17G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+17G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+17G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+17G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+17G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+17G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+17G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+17G>A
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14965
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7185
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum

7-750950-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750950
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750950
    reference: chr 7
allele count: 2
allele frequency: 1.669644198821231e-5
allele num: 119786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+16C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+16C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+16C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+16C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+16C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+16C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+16C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+16C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+16C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2939
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22162
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3153
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4521
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

7-750951-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750951
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750951
    reference: chr 7
allele count: 6
allele frequency: 5.005255518294209e-5
allele num: 119874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+15C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+15C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+15C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+15C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+15C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+15C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+15C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+15C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+15C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 12220
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9330
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-750951-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750951
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750952
    reference: chr 7
allele count: 1
allele frequency: 8.342092530490349e-6
allele num: 119874
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+14_177+15insA
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+14_177+15insA
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+14_177+15insA
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+14_227+15insA
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+14_177+15insA
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+14_177+15insA
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+14_177+15insA
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+14_177+15insA
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+14_177+15insA
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1899
  bin: 8.75e1
  variant carriers: 0
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: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/7-750952-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750952
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750952
    reference: chr 7
allele count: 5
allele frequency: 4.169724464607379e-5
allele num: 119912
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+14G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+14G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+14G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+14G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+14G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+14G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+14G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+14G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+14G>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12274
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

7-750952-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750952
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750951
    reference: chr 7
allele count: 1
allele frequency: 8.339448929214757e-6
allele num: 119912
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+13delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+13delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+13delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+13delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+13delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+13delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+13delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+13delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+13delC
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22293
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 907
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: CG
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD

7-750953-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750953
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750953
    reference: chr 7
allele count: 2
allele frequency: 1.665084836072398e-5
allele num: 120114
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+13C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+13C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+13C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+13C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+13C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+13C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+13C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+13C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+13C>G
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12218
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7312
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

7-750954-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750954
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750954
    reference: chr 7
allele count: 1
allele frequency: 8.315593400745077e-6
allele num: 120256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+12C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+12C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+12C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+12C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+12C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+12C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+12C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+12C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+12C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7350
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4534
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

7-750956-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750956
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750956
    reference: chr 7
allele count: 1
allele frequency: 8.302062232258493e-6
allele num: 120452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+10C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+10C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+10C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+10C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+10C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+10C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+10C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+10C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+10C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12276
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3182
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23256
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-750957-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750957
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750957
    reference: chr 7
allele count: 1
allele frequency: 8.299719469481931e-6
allele num: 120486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+9C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+9C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+9C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+9C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+9C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+9C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+9C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+9C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+9C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3184
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/7-750958-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750958
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750958
    reference: chr 7
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+8G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+8G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+8G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+8G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+8G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+8G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+8G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+8G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+8G>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23259
  bin: 6.25e1
  variant carriers: 0
hgvs: c.177+8G>T
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

7-750960-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750960
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750960
    reference: chr 7
allele count: 2
allele frequency: 1.657577616071872e-5
allele num: 120658
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+6T>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+6T>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+6T>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+6T>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+6T>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+6T>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+6T>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+6T>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+6T>C
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9912
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3859
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
hgvs: c.177+6T>C
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

7-750961-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750961
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750961
    reference: chr 7
allele count: 1
allele frequency: 8.2847295864263e-6
allele num: 120704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.177+5G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.177+5G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.177+5G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.177+5G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.227+5G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.177+5G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.177+5G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.177+5G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.177+5G>A
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3189
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
hgvs: c.177+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-750978-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750978
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750978
    reference: chr 7
allele count: 3
allele frequency: 2.477864411259416e-5
allele num: 121072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.165G>A
  hgvsp: ENST00000360274.4:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.165G>A
  hgvsp: ENST00000417852.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.165G>A
  hgvsp: ENST00000403562.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.165G>A
  hgvsp: ENST00000537384.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.165G>A
  hgvsp: ENST00000406797.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.165G>A
  hgvsp: ENST00000544935.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.165G>A
  hgvsp: ENST00000456696.2:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.165G>A
  hgvsp: ENST00000430040.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.215G>A
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4550
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2936
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu55Glu
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

7-750981-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750981
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750981
    reference: chr 7
allele count: 2
allele frequency: 1.651064110819423e-5
allele num: 121134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.212C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.162C>G
  hgvsp: ENSP00000385349.1:p.Phe54Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.162C>G
  hgvsp: ENSP00000406670.1:p.Phe54Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.162C>G
  hgvsp: ENSP00000440449.1:p.Phe54Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.162C>G
  hgvsp: ENSP00000385749.1:p.Phe54Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.162C>G
  hgvsp: ENSP00000353415.4:p.Phe54Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.162C>G
  hgvsp: ENSP00000402648.1:p.Phe54Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.162C>G
  hgvsp: ENSP00000410414.2:p.Phe54Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.162C>G
  hgvsp: ENSP00000444487.1:p.Phe54Leu
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7503
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Phe54Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

7-750983-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750983
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750983
    reference: chr 7
allele count: 2
allele frequency: 1.650818806127839e-5
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.160T>A
  hgvsp: ENSP00000353415.4:p.Phe54Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.160T>A
  hgvsp: ENSP00000406670.1:p.Phe54Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.160T>A
  hgvsp: ENSP00000402648.1:p.Phe54Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.160T>A
  hgvsp: ENSP00000440449.1:p.Phe54Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.160T>A
  hgvsp: ENSP00000385349.1:p.Phe54Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.160T>A
  hgvsp: ENSP00000444487.1:p.Phe54Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.160T>A
  hgvsp: ENSP00000410414.2:p.Phe54Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.210T>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.160T>A
  hgvsp: ENSP00000385749.1:p.Phe54Ile
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3862
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12214
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7507
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Phe54Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

7-750985-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750985
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750985
    reference: chr 7
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.158A>G
  hgvsp: ENSP00000440449.1:p.His53Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.158A>G
  hgvsp: ENSP00000406670.1:p.His53Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.208A>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.158A>G
  hgvsp: ENSP00000402648.1:p.His53Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.158A>G
  hgvsp: ENSP00000353415.4:p.His53Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.158A>G
  hgvsp: ENSP00000385349.1:p.His53Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.158A>G
  hgvsp: ENSP00000385749.1:p.His53Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.158A>G
  hgvsp: ENSP00000410414.2:p.His53Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.158A>G
  hgvsp: ENSP00000444487.1:p.His53Arg
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24207
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3860
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3201
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His53Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

7-750986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750986
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750986
    reference: chr 7
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.157C>T
  hgvsp: ENSP00000385349.1:p.His53Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.207C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.157C>T
  hgvsp: ENSP00000406670.1:p.His53Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.157C>T
  hgvsp: ENSP00000385749.1:p.His53Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.157C>T
  hgvsp: ENSP00000353415.4:p.His53Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.157C>T
  hgvsp: ENSP00000402648.1:p.His53Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.157C>T
  hgvsp: ENSP00000410414.2:p.His53Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.157C>T
  hgvsp: ENSP00000444487.1:p.His53Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.157C>T
  hgvsp: ENSP00000440449.1:p.His53Tyr
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His53Tyr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

7-750987-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 750987
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 750987
    reference: chr 7
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.156G>A
  hgvsp: ENST00000544935.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.156G>A
  hgvsp: ENST00000537384.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.156G>A
  hgvsp: ENST00000406797.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.156G>A
  hgvsp: ENST00000417852.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.206G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.156G>A
  hgvsp: ENST00000430040.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.156G>A
  hgvsp: ENST00000403562.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.156G>A
  hgvsp: ENST00000456696.2:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.156G>A
  hgvsp: ENST00000360274.4:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7896
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3204
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu52Glu
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/7-751009-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751009
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751009
    reference: chr 7
allele count: 4
allele frequency: 3.29733740004946e-5
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.134G>T
  hgvsp: ENSP00000440449.1:p.Arg45Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.134G>T
  hgvsp: ENSP00000410414.2:p.Arg45Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.184G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.134G>T
  hgvsp: ENSP00000444487.1:p.Arg45Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.134G>T
  hgvsp: ENSP00000402648.1:p.Arg45Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.134G>T
  hgvsp: ENSP00000385349.1:p.Arg45Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.134G>T
  hgvsp: ENSP00000353415.4:p.Arg45Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.134G>T
  hgvsp: ENSP00000406670.1:p.Arg45Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.134G>T
  hgvsp: ENSP00000385749.1:p.Arg45Leu
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2936
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24363
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg45Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

7-751013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751013
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751013
    reference: chr 7
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.180G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.130G>A
  hgvsp: ENSP00000406670.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.130G>A
  hgvsp: ENSP00000444487.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.130G>A
  hgvsp: ENSP00000385349.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.130G>A
  hgvsp: ENSP00000440449.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.130G>A
  hgvsp: ENSP00000353415.4:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.130G>A
  hgvsp: ENSP00000410414.2:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.130G>A
  hgvsp: ENSP00000385749.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.130G>A
  hgvsp: ENSP00000402648.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu44Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

7-751014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751014
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751014
    reference: chr 7
allele count: 6
allele frequency: 4.945843018942579e-5
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.129C>T
  hgvsp: ENST00000403562.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.179C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.129C>T
  hgvsp: ENST00000417852.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.129C>T
  hgvsp: ENST00000537384.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.129C>T
  hgvsp: ENST00000430040.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.129C>T
  hgvsp: ENST00000406797.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.129C>T
  hgvsp: ENST00000456696.2:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.129C>T
  hgvsp: ENST00000360274.4:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.129C>T
  hgvsp: ENST00000544935.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1899
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro43Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

7-751021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751021
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751021
    reference: chr 7
allele count: 5
allele frequency: 4.120856478810556e-5
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.172C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.122C>T
  hgvsp: ENSP00000385349.1:p.Ser41Phe
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.122C>T
  hgvsp: ENSP00000444487.1:p.Ser41Phe
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.122C>T
  hgvsp: ENSP00000385749.1:p.Ser41Phe
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.122C>T
  hgvsp: ENSP00000353415.4:p.Ser41Phe
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.122C>T
  hgvsp: ENSP00000406670.1:p.Ser41Phe
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.122C>T
  hgvsp: ENSP00000402648.1:p.Ser41Phe
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.122C>T
  hgvsp: ENSP00000440449.1:p.Ser41Phe
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.122C>T
  hgvsp: ENSP00000410414.2:p.Ser41Phe
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16202
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7532
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser41Phe
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

7-751025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751025
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751025
    reference: chr 7
allele count: 895
allele frequency: 7.376089930607064e-3
allele num: 121338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.118A>G
  hgvsp: ENSP00000440449.1:p.Ile40Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.118A>G
  hgvsp: ENSP00000402648.1:p.Ile40Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.118A>G
  hgvsp: ENSP00000410414.2:p.Ile40Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.118A>G
  hgvsp: ENSP00000353415.4:p.Ile40Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.118A>G
  hgvsp: ENSP00000385349.1:p.Ile40Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.118A>G
  hgvsp: ENSP00000444487.1:p.Ile40Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.118A>G
  hgvsp: ENSP00000406670.1:p.Ile40Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.168A>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.118A>G
  hgvsp: ENSP00000385749.1:p.Ile40Val
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16081
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 5.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10015
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 435
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12300
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7796
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12583
  bin: 9.75e1
  variant carriers: 881
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile40Val
num of homozygotes: 14
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

7-751026-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751026
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751026
    reference: chr 7
allele count: 3
allele frequency: 2.472269378471478e-5
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.167C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.117C>G
  hgvsp: ENSP00000406670.1:p.Cys39Trp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.117C>G
  hgvsp: ENSP00000385749.1:p.Cys39Trp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.117C>G
  hgvsp: ENSP00000402648.1:p.Cys39Trp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.117C>G
  hgvsp: ENSP00000385349.1:p.Cys39Trp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.117C>G
  hgvsp: ENSP00000444487.1:p.Cys39Trp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.117C>G
  hgvsp: ENSP00000440449.1:p.Cys39Trp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.117C>G
  hgvsp: ENSP00000353415.4:p.Cys39Trp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.117C>G
  hgvsp: ENSP00000410414.2:p.Cys39Trp
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4580
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7586
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Cys39Trp
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

7-751034-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751034
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751034
    reference: chr 7
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.109C>A
  hgvsp: ENSP00000385349.1:p.His37Asn
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.109C>A
  hgvsp: ENSP00000353415.4:p.His37Asn
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.109C>A
  hgvsp: ENSP00000444487.1:p.His37Asn
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.109C>A
  hgvsp: ENSP00000440449.1:p.His37Asn
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.109C>A
  hgvsp: ENSP00000402648.1:p.His37Asn
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.109C>A
  hgvsp: ENSP00000406670.1:p.His37Asn
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.159C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.109C>A
  hgvsp: ENSP00000385749.1:p.His37Asn
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.109C>A
  hgvsp: ENSP00000410414.2:p.His37Asn
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His37Asn
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

7-751037-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751037
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751037
    reference: chr 7
allele count: 8
allele frequency: 6.592501030078285e-5
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.106G>A
  hgvsp: ENSP00000353415.4:p.Val36Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.106G>A
  hgvsp: ENSP00000444487.1:p.Val36Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.156G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.106G>A
  hgvsp: ENSP00000385349.1:p.Val36Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.106G>A
  hgvsp: ENSP00000402648.1:p.Val36Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.106G>A
  hgvsp: ENSP00000406670.1:p.Val36Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.106G>A
  hgvsp: ENSP00000385749.1:p.Val36Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.106G>A
  hgvsp: ENSP00000440449.1:p.Val36Ile
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.106G>A
  hgvsp: ENSP00000410414.2:p.Val36Ile
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16389
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val36Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

7-751038-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751038
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751038
    reference: chr 7
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.105C>G
  hgvsp: ENSP00000385349.1:p.Ile35Met
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.105C>G
  hgvsp: ENSP00000410414.2:p.Ile35Met
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.105C>G
  hgvsp: ENSP00000353415.4:p.Ile35Met
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.105C>G
  hgvsp: ENSP00000444487.1:p.Ile35Met
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.105C>G
  hgvsp: ENSP00000402648.1:p.Ile35Met
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.155C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.105C>G
  hgvsp: ENSP00000440449.1:p.Ile35Met
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.105C>G
  hgvsp: ENSP00000385749.1:p.Ile35Met
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.105C>G
  hgvsp: ENSP00000406670.1:p.Ile35Met
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11855
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile35Met
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

7-751042-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751042
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751042
    reference: chr 7
allele count: 5
allele frequency: 4.120109430106464e-5
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.101G>A
  hgvsp: ENSP00000353415.4:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.101G>A
  hgvsp: ENSP00000385749.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.101G>A
  hgvsp: ENSP00000444487.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.101G>A
  hgvsp: ENSP00000402648.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.101G>A
  hgvsp: ENSP00000410414.2:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.101G>A
  hgvsp: ENSP00000385349.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.101G>A
  hgvsp: ENSP00000406670.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.151G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.101G>A
  hgvsp: ENSP00000440449.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24678
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Cys34Tyr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-751052-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751052
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751052
    reference: chr 7
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.91C>G
  hgvsp: ENSP00000385349.1:p.Leu31Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.91C>G
  hgvsp: ENSP00000410414.2:p.Leu31Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.91C>G
  hgvsp: ENSP00000385749.1:p.Leu31Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.141C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.91C>G
  hgvsp: ENSP00000402648.1:p.Leu31Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.91C>G
  hgvsp: ENSP00000444487.1:p.Leu31Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.91C>G
  hgvsp: ENSP00000440449.1:p.Leu31Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.91C>G
  hgvsp: ENSP00000406670.1:p.Leu31Val
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.91C>G
  hgvsp: ENSP00000353415.4:p.Leu31Val
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu31Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

7-751065-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751065
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751065
    reference: chr 7
allele count: 5
allele frequency: 4.120992334954257e-5
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.78G>A
  hgvsp: ENST00000537384.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.78G>A
  hgvsp: ENST00000360274.4:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.78G>A
  hgvsp: ENST00000406797.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.78G>A
  hgvsp: ENST00000544935.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.128G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.78G>A
  hgvsp: ENST00000430040.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.78G>A
  hgvsp: ENST00000403562.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.78G>A
  hgvsp: ENST00000417852.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.78G>A
  hgvsp: ENST00000456696.2:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly26Gly
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

7-751067-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751067
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751067
    reference: chr 7
allele count: 6
allele frequency: 4.945516888940176e-5
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.76G>A
  hgvsp: ENSP00000444487.1:p.Gly26Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.76G>A
  hgvsp: ENSP00000440449.1:p.Gly26Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.76G>A
  hgvsp: ENSP00000385749.1:p.Gly26Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.76G>A
  hgvsp: ENSP00000353415.4:p.Gly26Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.76G>A
  hgvsp: ENSP00000385349.1:p.Gly26Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.76G>A
  hgvsp: ENSP00000402648.1:p.Gly26Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.126G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.76G>A
  hgvsp: ENSP00000406670.1:p.Gly26Arg
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.76G>A
  hgvsp: ENSP00000410414.2:p.Gly26Arg
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4580
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly26Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

7-751079-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751079
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751079
    reference: chr 7
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.64G>C
  hgvsp: ENSP00000353415.4:p.Val22Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.64G>C
  hgvsp: ENSP00000444487.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.64G>C
  hgvsp: ENSP00000402648.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.64G>C
  hgvsp: ENSP00000440449.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.64G>C
  hgvsp: ENSP00000406670.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.64G>C
  hgvsp: ENSP00000385749.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.64G>C
  hgvsp: ENSP00000410414.2:p.Val22Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.64G>C
  hgvsp: ENSP00000385349.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.114G>C
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val22Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

7-751080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751080
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751080
    reference: chr 7
allele count: 7
allele frequency: 5.771387111668096e-5
allele num: 121288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.63C>T
  hgvsp: ENST00000403562.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.63C>T
  hgvsp: ENST00000537384.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.63C>T
  hgvsp: ENST00000417852.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.63C>T
  hgvsp: ENST00000430040.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.63C>T
  hgvsp: ENST00000360274.4:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.63C>T
  hgvsp: ENST00000406797.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.63C>T
  hgvsp: ENST00000456696.2:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.113C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.63C>T
  hgvsp: ENST00000544935.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24575
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3860
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr21Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-751094-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751094
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751094
    reference: chr 7
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.49G>T
  hgvsp: ENSP00000410414.2:p.Gly17Cys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.49G>T
  hgvsp: ENSP00000353415.4:p.Gly17Cys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.49G>T
  hgvsp: ENSP00000402648.1:p.Gly17Cys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.49G>T
  hgvsp: ENSP00000385749.1:p.Gly17Cys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.49G>T
  hgvsp: ENSP00000440449.1:p.Gly17Cys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.49G>T
  hgvsp: ENSP00000406670.1:p.Gly17Cys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.99G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.49G>T
  hgvsp: ENSP00000385349.1:p.Gly17Cys
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.49G>T
  hgvsp: ENSP00000444487.1:p.Gly17Cys
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly17Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

7-751104-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751104
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751104
    reference: chr 7
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.39G>C
  hgvsp: ENSP00000385749.1:p.Glu13Asp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.39G>C
  hgvsp: ENSP00000444487.1:p.Glu13Asp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.39G>C
  hgvsp: ENSP00000385349.1:p.Glu13Asp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.39G>C
  hgvsp: ENSP00000402648.1:p.Glu13Asp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.39G>C
  hgvsp: ENSP00000440449.1:p.Glu13Asp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.39G>C
  hgvsp: ENSP00000406670.1:p.Glu13Asp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.89G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.39G>C
  hgvsp: ENSP00000353415.4:p.Glu13Asp
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.39G>C
  hgvsp: ENSP00000410414.2:p.Glu13Asp
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu13Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

7-751107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751107
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751107
    reference: chr 7
allele count: 2
allele frequency: 1.651718613217052e-5
allele num: 121086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.36C>T
  hgvsp: ENST00000360274.4:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.36C>T
  hgvsp: ENST00000403562.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.36C>T
  hgvsp: ENST00000417852.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.36C>T
  hgvsp: ENST00000406797.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.36C>T
  hgvsp: ENST00000544935.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.36C>T
  hgvsp: ENST00000456696.2:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.36C>T
  hgvsp: ENST00000537384.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.86C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.36C>T
  hgvsp: ENST00000430040.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12509
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp12Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-751114-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751114
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751114
    reference: chr 7
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.29A>G
  hgvsp: ENSP00000385749.1:p.Glu10Gly
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.29A>G
  hgvsp: ENSP00000440449.1:p.Glu10Gly
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.29A>G
  hgvsp: ENSP00000402648.1:p.Glu10Gly
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.29A>G
  hgvsp: ENSP00000353415.4:p.Glu10Gly
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.29A>G
  hgvsp: ENSP00000385349.1:p.Glu10Gly
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.29A>G
  hgvsp: ENSP00000406670.1:p.Glu10Gly
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.29A>G
  hgvsp: ENSP00000410414.2:p.Glu10Gly
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.79A>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.29A>G
  hgvsp: ENSP00000444487.1:p.Glu10Gly
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu10Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/7-751115-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751115
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751115
    reference: chr 7
allele count: 1
allele frequency: 8.265282507356101e-6
allele num: 120988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.28G>T
  hgvsp: ENSP00000406670.1:p.Glu10Ter
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.28G>T
  hgvsp: ENSP00000385749.1:p.Glu10Ter
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.28G>T
  hgvsp: ENSP00000353415.4:p.Glu10Ter
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.28G>T
  hgvsp: ENSP00000402648.1:p.Glu10Ter
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.28G>T
  hgvsp: ENSP00000444487.1:p.Glu10Ter
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.28G>T
  hgvsp: ENSP00000385349.1:p.Glu10Ter
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.28G>T
  hgvsp: ENSP00000440449.1:p.Glu10Ter
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.78G>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.28G>T
  hgvsp: ENSP00000410414.2:p.Glu10Ter
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu10Ter
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

7-751116-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751116
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751116
    reference: chr 7
allele count: 1
allele frequency: 8.266649031148734e-6
allele num: 120968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.27G>A
  hgvsp: ENST00000544935.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.27G>A
  hgvsp: ENST00000406797.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.27G>A
  hgvsp: ENST00000417852.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.27G>A
  hgvsp: ENST00000537384.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.27G>A
  hgvsp: ENST00000430040.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.77G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.27G>A
  hgvsp: ENST00000403562.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.27G>A
  hgvsp: ENST00000360274.4:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.27G>A
  hgvsp: ENST00000456696.2:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser9Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

7-751127-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751127
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751126
    reference: chr 7
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.15delC
  hgvsp: ENSP00000402648.1:p.Ala6ProfsTer10
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.15delC
  hgvsp: ENSP00000385749.1:p.Ala6ProfsTer10
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.15delC
  hgvsp: ENSP00000440449.1:p.Ala6ProfsTer10
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.15delC
  hgvsp: ENSP00000410414.2:p.Ala6ProfsTer10
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.15delC
  hgvsp: ENSP00000444487.1:p.Ala6ProfsTer10
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.15delC
  hgvsp: ENSP00000406670.1:p.Ala6ProfsTer10
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.15delC
  hgvsp: ENSP00000385349.1:p.Ala6ProfsTer10
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.15delC
  hgvsp: ENSP00000353415.4:p.Ala6ProfsTer10
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.65delC
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 12475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16032
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala6ProfsTer10
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: CG
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

7-751132-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751132
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751132
    reference: chr 7
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.11C>T
  hgvsp: ENSP00000410414.2:p.Pro4Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.61C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.11C>T
  hgvsp: ENSP00000353415.4:p.Pro4Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.11C>T
  hgvsp: ENSP00000440449.1:p.Pro4Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.11C>T
  hgvsp: ENSP00000402648.1:p.Pro4Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.11C>T
  hgvsp: ENSP00000444487.1:p.Pro4Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.11C>T
  hgvsp: ENSP00000406670.1:p.Pro4Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.11C>T
  hgvsp: ENSP00000385349.1:p.Pro4Leu
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.11C>T
  hgvsp: ENSP00000385749.1:p.Pro4Leu
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro4Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

7-751145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751145
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751145
    reference: chr 7
allele count: 1
allele frequency: 8.332777814812346e-6
allele num: 120008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.-3G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.48G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.-3G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3827
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11831
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

7-751150-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751150
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751150
    reference: chr 7
allele count: 4
allele frequency: 3.337505214851898e-5
allele num: 119850
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.-8C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-8C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.-8C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.-8C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-8C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-8C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.43C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.-8C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.-8C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4490
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

7-751151-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751151
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751151
    reference: chr 7
allele count: 1
allele frequency: 8.353102342209896e-6
allele num: 119716
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.-9A>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.-9A>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.42A>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.-9A>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-9A>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-9A>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.-9A>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-9A>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.-9A>G
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3815
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3078
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

7-751183-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751183
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751183
    reference: chr 7
allele count: 1
allele frequency: 8.492569002123141e-6
allele num: 117750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.-22-19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-22-19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.29-19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-22-19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-22-19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.-22-19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.-22-19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.-22-19C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.-22-19C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11197
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4219
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5716
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2500
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2873
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1832
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2797
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

7-751188-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751188
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751188
    reference: chr 7
allele count: 1
allele frequency: 8.534753516318448e-6
allele num: 117168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.-22-24G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-22-24G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.29-24G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.-22-24G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-22-24G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-22-24G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.-22-24G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.-22-24G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.-22-24G>C
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3232
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2387
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2747
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2781
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

7-751190-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751190
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751189
    reference: chr 7
allele count: 1
allele frequency: 8.554173581290312e-6
allele num: 116902
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.-22-27delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.-22-27delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.-22-27delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-22-27delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-22-27delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.29-27delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-22-27delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.-22-27delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.-22-27delC
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1822
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4139
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3677
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: AG
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-751191-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 751191
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 751191
    reference: chr 7
allele count: 1
allele frequency: 8.552125203112974e-6
allele num: 116930
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-22-27C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000410414
  ensembl transcript: ENST00000456696
  gene symbol: PRKAR1B
  hgvsc: ENST00000456696.2:c.-22-27C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-22-27C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000444487
  ensembl transcript: ENST00000544935
  gene symbol: PRKAR1B
  hgvsc: ENST00000544935.1:c.-22-27C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000353415
  ensembl transcript: ENST00000360274
  gene symbol: PRKAR1B
  hgvsc: ENST00000360274.4:c.-22-27C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000402648
  ensembl transcript: ENST00000430040
  gene symbol: PRKAR1B
  hgvsc: ENST00000430040.1:c.-22-27C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.29-27C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385749
  ensembl transcript: ENST00000406797
  gene symbol: PRKAR1B
  hgvsc: ENST00000406797.1:c.-22-27C>G
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-22-27C>G
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7959
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1682
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1674
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS

7-766307-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 766307
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 766307
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 24
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.28+540G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-23+540G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000478198
  gene symbol: PRKAR1B
  hgvsc: ENST00000478198.1:n.308G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-23+920G>C
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-23+540G>C
  variant of: http://identifiers.org/hgnc/9390
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3701
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2876
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

7-766426-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 766426
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 766426
    reference: chr 7
allele count: 1
allele frequency: 1.282051282051282e-2
allele num: 78
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-23+421C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-23+421C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000321451
  ensembl transcript: ENST00000313147
  gene symbol: HEATR2
  hgvsc: ENST00000313147.5:c.69G>T
  hgvsp: ENSP00000321451.5:p.Glu23Asp
  variant of: http://identifiers.org/hgnc/26013
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000478198
  gene symbol: PRKAR1B
  hgvsc: ENST00000478198.1:n.189C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000297440
  ensembl transcript: ENST00000297440
  gene symbol: HEATR2
  hgvsc: ENST00000297440.6:c.69G>T
  hgvsp: ENSP00000297440.6:p.Glu23Asp
  variant of: http://identifiers.org/hgnc/26013
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.28+421C>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-23+801C>A
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4274
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu23Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

7-766429-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 766429
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 766429
    reference: chr 7
allele count: 6
allele frequency: 5.454545454545454e-2
allele num: 110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.28+418C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-23+418C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000478198
  gene symbol: PRKAR1B
  hgvsc: ENST00000478198.1:n.186C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-23+418C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-23+798C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000321451
  ensembl transcript: ENST00000313147
  gene symbol: HEATR2
  hgvsc: ENST00000313147.5:c.72G>A
  hgvsp: ENST00000313147.5:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26013
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000297440
  ensembl transcript: ENST00000297440
  gene symbol: HEATR2
  hgvsc: ENST00000297440.6:c.72G>A
  hgvsp: ENST00000297440.6:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26013
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4068
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 2
hgvs: p.Ala24Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

7-766438-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 766438
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 766438
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000321451
  ensembl transcript: ENST00000313147
  gene symbol: HEATR2
  hgvsc: ENST00000313147.5:c.81G>A
  hgvsp: ENST00000313147.5:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26013
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000478198
  gene symbol: PRKAR1B
  hgvsc: ENST00000478198.1:n.177C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000297440
  ensembl transcript: ENST00000297440
  gene symbol: HEATR2
  hgvsc: ENST00000297440.6:c.81G>A
  hgvsp: ENST00000297440.6:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26013
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-23+409C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.28+409C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-23+409C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-23+789C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu27Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

7-766470-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 766470
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 766469
    reference: chr 7
allele count: 1
allele frequency: 2.136752136752137e-3
allele num: 468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-23+756delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-23+376delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-23+376delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000297440
  ensembl transcript: ENST00000297440
  gene symbol: HEATR2
  hgvsc: ENST00000297440.6:c.115delG
  hgvsp: ENSP00000297440.6:p.Glu39ArgfsTer47
  variant of: http://identifiers.org/hgnc/26013
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000321451
  ensembl transcript: ENST00000313147
  gene symbol: HEATR2
  hgvsc: ENST00000313147.5:c.115delG
  hgvsp: ENSP00000321451.5:p.Glu39ArgfsTer47
  variant of: http://identifiers.org/hgnc/26013
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000478198
  gene symbol: PRKAR1B
  hgvsc: ENST00000478198.1:n.144delC
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.28+376delC
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1550
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu39ArgfsTer47
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: TG
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

7-766482-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 766482
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 766482
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000478198
  gene symbol: PRKAR1B
  hgvsc: ENST00000478198.1:n.133C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000297440
  ensembl transcript: ENST00000297440
  gene symbol: HEATR2
  hgvsc: ENST00000297440.6:c.125G>A
  hgvsp: ENSP00000297440.6:p.Ser42Asn
  variant of: http://identifiers.org/hgnc/26013
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-23+745C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-23+365C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000321451
  ensembl transcript: ENST00000313147
  gene symbol: HEATR2
  hgvsc: ENST00000313147.5:c.125G>A
  hgvsp: ENSP00000321451.5:p.Ser42Asn
  variant of: http://identifiers.org/hgnc/26013
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.28+365C>T
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-23+365C>T
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2703
  bin: 7.5e0
  variant carriers: 1
hgvs: p.Ser42Asn
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

7-766558-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 766558
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 766558
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 1720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000406670
  ensembl transcript: ENST00000417852
  gene symbol: PRKAR1B
  hgvsc: ENST00000417852.1:c.-23+289G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000440449
  ensembl transcript: ENST00000537384
  gene symbol: PRKAR1B
  hgvsc: ENST00000537384.1:c.-23+289G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000321451
  ensembl transcript: ENST00000313147
  gene symbol: HEATR2
  hgvsc: ENST00000313147.5:c.201C>T
  hgvsp: ENST00000313147.5:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26013
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000478198
  gene symbol: PRKAR1B
  hgvsc: ENST00000478198.1:n.57G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164818
  ensembl protein: ENSP00000297440
  ensembl transcript: ENST00000297440
  gene symbol: HEATR2
  hgvsc: ENST00000297440.6:c.201C>T
  hgvsp: ENST00000297440.6:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26013
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl protein: ENSP00000385349
  ensembl transcript: ENST00000403562
  gene symbol: PRKAR1B
  hgvsc: ENST00000403562.1:c.-23+669G>A
  variant of: http://identifiers.org/hgnc/9390
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188191
  ensembl transcript: ENST00000488474
  gene symbol: PRKAR1B
  hgvsc: ENST00000488474.1:n.28+289G>A
  variant of: http://identifiers.org/hgnc/9390
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15668
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15379
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3039
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr67Thr
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 619
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 109
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5341
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 750
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.494505494505495e-3
allele num: 182
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.49e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.31152e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.229e1

VQSLOD
type: SiteQuality
SIO_000300: 3.95e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 897
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 9.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 9
allele frequency: 8.490566037735849e-3
allele num: 1060
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.620082427875609e-4
allele num: 5338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 942
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.075e1

FS
type: SiteQuality
SIO_000300: 5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.47e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.30025e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

GenotypeQuality
all individuals: 208
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2776
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 115
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5341
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.882530120481928e-4
allele num: 5312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 940
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.424e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.58e-2

FS
type: SiteQuality
SIO_000300: 3.217e0

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

DP
type: SiteQuality
SIO_000300: 4.29133e5

MQRankSum
type: SiteQuality
SIO_000300: 5.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 174
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5341
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 124
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.765060240963856e-4
allele num: 5312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1010
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.127659574468085e-3
allele num: 940
num of homozygotes: 1

South Asian
type: Population
allele count: 1
allele frequency: 1.304461257500652e-4
allele num: 7666
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.58e-2

FS
type: SiteQuality
SIO_000300: 3.217e0

QD
type: SiteQuality
SIO_000300: 1.424e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.11e-1

DP
type: SiteQuality
SIO_000300: 4.29133e5

GenotypeQuality
all individuals: 978
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5339
bin: 9.75e1
variant carriers: 8

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.322251605591235e-3
allele num: 5294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.304461257500652e-4
allele num: 7666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 1.258e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.17e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-1

DP
type: SiteQuality
SIO_000300: 4.27548e5

MQRankSum
type: SiteQuality
SIO_000300: 5.11e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

MQ
type: SiteQuality
SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

GenotypeQuality
all individuals: 1311
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4553
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3892
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15844
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 253
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1908
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65036
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.688097306689835e-5
allele num: 11510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15514
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.802e1

DP
type: SiteQuality
SIO_000300: 1.950814e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.196e0

FS
type: SiteQuality
SIO_000300: 4.482e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.454e0

VQSLOD
type: SiteQuality
SIO_000300: -9.026e-1

GenotypeQuality
all individuals: 12458
bin: 9.75e1
variant carriers: 271

GenotypeQuality
all individuals: 16696
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 150
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2937
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1893
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 148
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3105
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3854
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4510
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 707
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 619
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.718034473887317e-4
allele num: 15548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 66
allele frequency: 1.028357743845435e-2
allele num: 6418
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.813856572321583e-4
allele num: 11518
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.991219317501497e-4
allele num: 10022
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.416856492027335e-3
allele num: 878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 189
allele frequency: 2.904118008604794e-3
allele num: 65080
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 7.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.04e0

DP
type: SiteQuality
SIO_000300: 1.954277e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.667e0

QD
type: SiteQuality
SIO_000300: 1.265e1

GenotypeQuality
all individuals: 637
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.552795031055901e-4
allele num: 6440
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10052
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.204712812960235e-5
allele num: 65184
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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.19e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

DP
type: SiteQuality
SIO_000300: 1.959364e6

FS
type: SiteQuality
SIO_000300: 1.462e0

VQSLOD
type: SiteQuality
SIO_000300: 9.06e-1

QD
type: SiteQuality
SIO_000300: 1.174e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.067108330266225e-5
allele num: 65208
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10066
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

FS
type: SiteQuality
SIO_000300: 2.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.963933e6

QD
type: SiteQuality
SIO_000300: 1.136e1

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-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: 8.25e1
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East Asian
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allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.598123965422108e-5
allele num: 65244
num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.551831160769708e-4
allele num: 6444
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.241e1

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.74e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.969003e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.85e-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: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.304375236414071e-5
allele num: 15862
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.987795e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.838e0

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

QD
type: SiteQuality
SIO_000300: 9.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.34e-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

South Asian
type: Population
allele count: 1
allele frequency: 6.2266500622665e-5
allele num: 16060
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65708
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.000254e6

QD
type: SiteQuality
SIO_000300: 7.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

MQRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.13e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.96e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.24e-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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521282745611099e-5
allele num: 65734
num of homozygotes: 0

South Asian
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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DP
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
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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allele count: 1
allele frequency: 1.521005080156968e-5
allele num: 65746
num of homozygotes: 0

South Asian
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.064e0

MQ
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

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: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.521005080156968e-5
allele num: 65746
num of homozygotes: 0

European (Finnish)
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allele num: 6486
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Latino
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num of homozygotes: 0

South Asian
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allele frequency: 6.215813028344107e-5
allele num: 16088
num of homozygotes: 0

African
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East Asian
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Other
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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East Asian
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African
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allele frequency: 1.957330201605011e-4
allele num: 10218
num of homozygotes: 0

Latino
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European (Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
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QD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -5.610000000000001e-1

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.10719164566953e-5
allele num: 65882
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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BaseQRankSum
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MQ
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QD
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FS
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VQSLOD
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DP
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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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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Latino
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allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.517865274278255e-5
allele num: 65882
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6498
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Other
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allele num: 886
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FS
type: SiteQuality
SIO_000300: 1.0496e1

MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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MQ
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DP
type: SiteQuality
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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 (Finnish)
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allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.586332463433878e-5
allele num: 65908
num of homozygotes: 0

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

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

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.979e1

DP
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FS
type: SiteQuality
SIO_000300: 4.918e0

VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-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: 10230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517266492686776e-5
allele num: 65908
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16210
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.01271e6

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.384e1

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.030027573250917e-5
allele num: 66006
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Latino
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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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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East Asian
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European (Finnish)
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African
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allele num: 10276
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South Asian
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Other
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European (Non-Finnish)
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allele num: 66092
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Latino
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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QD
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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allele num: 11558
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African
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European (Non-Finnish)
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South Asian
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Other
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European (Finnish)
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ClippingRankSum
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MQ
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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DP
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FS
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InbreedingCoeff
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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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African
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele num: 66210
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Other
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South Asian
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European (Finnish)
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Latino
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.509798592867711e-5
allele num: 66234
num of homozygotes: 0

DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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SIO_000300: -3.117e0

FS
type: SiteQuality
SIO_000300: 2.524e0

QD
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InbreedingCoeff
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MQRankSum
type: SiteQuality
SIO_000300: 7.67e-1

VQSLOD
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SIO_000300: 5.639999999999999e-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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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.016773259321829e-5
allele num: 66296
num of homozygotes: 0

QD
type: SiteQuality
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MQ
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DP
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FS
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 6.6e-3

VQSLOD
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BaseQRankSum
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SIO_000300: -1.107e0

ClippingRankSum
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SIO_000300: -2.62e-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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.507886245061673e-5
allele num: 66318
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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QD
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SIO_000300: 1.303e1

BaseQRankSum
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SIO_000300: -1.389e0

VQSLOD
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ReadPosRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 6.22e-1

DP
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.509515076812073e-5
allele num: 66526
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.379e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.99e-1

MQRankSum
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.591e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 2.034875e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66562
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -9.186e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
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QD
type: SiteQuality
SIO_000300: 1.308e1

FS
type: SiteQuality
SIO_000300: 2.151e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.92e1

DP
type: SiteQuality
SIO_000300: 2.036028e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.977e0

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.004446580939791e-5
allele num: 66568
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European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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East Asian
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Latino
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DP
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ReadPosRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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QD
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GenotypeQuality
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variant carriers: 1

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

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

African
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.145e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
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SIO_000300: -4.9e-1

BaseQRankSum
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SIO_000300: -3.562e0

DP
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SIO_000300: 2.036918e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

FS
type: SiteQuality
SIO_000300: 3.312e0

VQSLOD
type: SiteQuality
SIO_000300: 9.63e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

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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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 3.456619426201175e-4
allele num: 11572
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e-1

FS
type: SiteQuality
SIO_000300: 3.181e0

ReadPosRankSum
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SIO_000300: -4.3e-2

DP
type: SiteQuality
SIO_000300: 2.039101e6

VQSLOD
type: SiteQuality
SIO_000300: 9.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

QD
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SIO_000300: 1.324e1

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

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
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: 8.76e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.8e-2

MQ
type: SiteQuality
SIO_000300: 5.939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 2.039083e6

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

Latino
type: Population
allele count: 6
allele frequency: 5.184929139301763e-4
allele num: 11572
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.96e-1

DP
type: SiteQuality
SIO_000300: 2.039473e6

QD
type: SiteQuality
SIO_000300: 1.363e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 3.18e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

MQRankSum
type: SiteQuality
SIO_000300: -3.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 10402
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: 6600
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.496701451361401e-5
allele num: 66696
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 8.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.568e0

MQRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 5.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

DP
type: SiteQuality
SIO_000300: 2.039547e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

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

Latino
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allele count: 91
allele frequency: 7.865168539325843e-3
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
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allele count: 236
allele frequency: 3.538230884557721e-3
allele num: 66700
num of homozygotes: 2

South Asian
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allele count: 45
allele frequency: 2.725620835857057e-3
allele num: 16510
num of homozygotes: 0

African
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allele count: 510
allele frequency: 4.902903287829263e-2
allele num: 10402
num of homozygotes: 12

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.544077552256892e-4
allele num: 6602
num of homozygotes: 0

DP
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SIO_000300: 2.087979e6

MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
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SIO_000300: 4.29e-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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

European (Finnish)
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allele count: 3
allele frequency: 4.544077552256892e-4
allele num: 6602
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ClippingRankSum
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SIO_000300: 3.52e-1

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

Other
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European (Finnish)
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499160470136723e-5
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Latino
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African
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East Asian
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VQSLOD
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QD
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FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.199328376109379e-4
allele num: 66704
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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East Asian
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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BaseQRankSum
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SIO_000300: 1.22e0

MQRankSum
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SIO_000300: 4.3e-2

FS
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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MQ
type: SiteQuality
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QD
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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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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

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

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

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

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

VQSLOD
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QD
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MQ
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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SIO_000300: -7.099999999999999e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 7.575757575757576e-4
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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MQ
type: SiteQuality
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MQRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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DP
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QD
type: SiteQuality
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InbreedingCoeff
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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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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: 6600
num of homozygotes: 0

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

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

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

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

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

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.614e0

MQRankSum
type: SiteQuality
SIO_000300: -7.34e-1

MQ
type: SiteQuality
SIO_000300: 5.99e1

InbreedingCoeff
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SIO_000300: 0.0e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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SIO_000300: 6.909999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.031914e6

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

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

East Asian
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allele count: 0
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allele num: 8648
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.592464569650881e-4
allele num: 11572
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

Other
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BaseQRankSum
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SIO_000300: -3.808e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.38e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.031656e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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MQRankSum
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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allele frequency: 7.498275396658768e-5
allele num: 66682
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Other
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African
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European (Finnish)
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allele num: 6600
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East Asian
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MQ
type: SiteQuality
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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African
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Other
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East Asian
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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BaseQRankSum
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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East Asian
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African
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Latino
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InbreedingCoeff
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MQ
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ClippingRankSum
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BaseQRankSum
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DP
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VQSLOD
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QD
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FS
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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African
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Other
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European (Non-Finnish)
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South Asian
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MQ
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.50253929140247e-5
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num of homozygotes: 0

African
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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QD
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MQRankSum
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MQ
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FS
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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ClippingRankSum
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SIO_000300: -9.9e-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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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
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Other
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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 num: 66534
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South Asian
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FS
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VQSLOD
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DP
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MQ
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MQRankSum
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QD
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6528
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Latino
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.503849855630414e-5
allele num: 66496
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African
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Other
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BaseQRankSum
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SIO_000300: 1.74e0

ClippingRankSum
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SIO_000300: 4.25e-1

MQ
type: SiteQuality
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VQSLOD
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DP
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QD
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FS
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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European (Non-Finnish)
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allele num: 66484
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Other
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ReadPosRankSum
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SIO_000300: 1.1e-1

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

East Asian
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num of homozygotes: 0

Latino
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African
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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MQ
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VQSLOD
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MQRankSum
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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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European (Non-Finnish)
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allele num: 66028
num of homozygotes: 0

Latino
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African
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South Asian
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European (Finnish)
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Other
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East Asian
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ReadPosRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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FS
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DP
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QD
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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Other
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East Asian
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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allele frequency: 6.06501698204755e-5
allele num: 65952
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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FS
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MQRankSum
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DP
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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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South Asian
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allele num: 16268
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.517542794706811e-5
allele num: 65896
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African
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Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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VQSLOD
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FS
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QD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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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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European (Non-Finnish)
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Other
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.733624454148471e-5
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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MQ
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 6112
num of homozygotes: 0

South Asian
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African
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 64650
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East Asian
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Other
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MQ
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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MQRankSum
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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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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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Latino
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East Asian
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African
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MQ
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BaseQRankSum
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FS
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MQRankSum
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QD
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ReadPosRankSum
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DP
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VQSLOD
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ClippingRankSum
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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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Latino
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South Asian
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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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Other
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MQ
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ClippingRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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FS
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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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East Asian
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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QD
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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DP
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ReadPosRankSum
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BaseQRankSum
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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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European (Non-Finnish)
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South Asian
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Other
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East Asian
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European (Finnish)
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African
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MQ
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BaseQRankSum
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FS
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DP
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MQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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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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South Asian
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East Asian
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Other
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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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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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East Asian
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allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.42e-2

DP
type: SiteQuality
SIO_000300: 1.8311e4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.577e0

MQRankSum
type: SiteQuality
SIO_000300: -1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 4.84e0

GenotypeQuality
all individuals: 2979
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.538071065989848e-3
allele num: 394
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.2758e4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.866e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

QD
type: SiteQuality
SIO_000300: 6.4e0

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.24e-2

MQ
type: SiteQuality
SIO_000300: 6.107e1

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 2.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 219
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.71e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.09e0

DP
type: SiteQuality
SIO_000300: 2.1908e4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.311e1

GenotypeQuality
all individuals: 305
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 388
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0