3-42576547-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576547
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576547
    reference: chr 3
allele count: 4
allele frequency: 3.294784356363876e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*590T>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*847T>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.968T>G
  hgvsp: ENSP00000394950.1:p.Phe323Cys
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.947T>G
  hgvsp: ENSP00000445701.1:p.Phe316Cys
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1091T>G
  hgvsp: ENSP00000327246.4:p.Phe364Cys
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.461T>G
  hgvsp: ENSP00000415371.2:p.Phe154Cys
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2190T>G
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26861
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4380
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe364Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

3-42576548-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576548
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576548
    reference: chr 3
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*591T>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2191T>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.948T>G
  hgvsp: ENSP00000445701.1:p.Phe316Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.969T>G
  hgvsp: ENSP00000394950.1:p.Phe323Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.462T>G
  hgvsp: ENSP00000415371.2:p.Phe154Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1092T>G
  hgvsp: ENSP00000327246.4:p.Phe364Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*848T>G
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4073
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26860
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe364Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

3-42576553-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576553
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576553
    reference: chr 3
allele count: 14
allele frequency: 1.153193522347243e-4
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*853C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1097C>T
  hgvsp: ENSP00000327246.4:p.Pro366Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.467C>T
  hgvsp: ENSP00000415371.2:p.Pro156Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.974C>T
  hgvsp: ENSP00000394950.1:p.Pro325Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2196C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.953C>T
  hgvsp: ENSP00000445701.1:p.Pro318Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*596C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4287
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro366Leu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

3-42576554-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576554
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576554
    reference: chr 3
allele count: 3
allele frequency: 2.471128976458378e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*854T>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.954T>G
  hgvsp: ENST00000543411.1:c.954T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.468T>G
  hgvsp: ENST00000438259.2:c.468T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.975T>G
  hgvsp: ENST00000433647.1:c.975T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1098T>G
  hgvsp: ENST00000325123.4:c.1098T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*597T>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2197T>G
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4377
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4287
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4073
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10614
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro366Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

3-42576573-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576573
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576572
    reference: chr 3
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.488delA
  hgvsp: ENSP00000415371.2:p.Glu163GlyfsTer27
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*874delA
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.995delA
  hgvsp: ENSP00000394950.1:p.Glu332GlyfsTer27
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2217delA
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1118delA
  hgvsp: ENSP00000327246.4:p.Glu373GlyfsTer27
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.974delA
  hgvsp: ENSP00000445701.1:p.Glu325GlyfsTer27
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*617delA
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4377
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu373GlyfsTer27
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: GA
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

3-42576576-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576576
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576576
    reference: chr 3
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.976C>T
  hgvsp: ENSP00000445701.1:p.Leu326Phe
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.490C>T
  hgvsp: ENSP00000415371.2:p.Leu164Phe
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1120C>T
  hgvsp: ENSP00000327246.4:p.Leu374Phe
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.997C>T
  hgvsp: ENSP00000394950.1:p.Leu333Phe
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*876C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2219C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*619C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10563
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu374Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

3-42576579-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576579
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576579
    reference: chr 3
allele count: 5
allele frequency: 4.119294776734223e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.493G>A
  hgvsp: ENSP00000415371.2:p.Val165Ile
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.979G>A
  hgvsp: ENSP00000445701.1:p.Val327Ile
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2222G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1000G>A
  hgvsp: ENSP00000394950.1:p.Val334Ile
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*879G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1123G>A
  hgvsp: ENSP00000327246.4:p.Val375Ile
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*622G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10887
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10551
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4072
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4373
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val375Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD

3-42576579-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576579
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576579
    reference: chr 3
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*879G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2222G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1000G>C
  hgvsp: ENSP00000394950.1:p.Val334Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1123G>C
  hgvsp: ENSP00000327246.4:p.Val375Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.979G>C
  hgvsp: ENSP00000445701.1:p.Val327Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.493G>C
  hgvsp: ENSP00000415371.2:p.Val165Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*622G>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4285
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4373
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2810
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2990
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val375Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ

3-42576582-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576582
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576582
    reference: chr 3
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*882G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1003G>A
  hgvsp: ENSP00000394950.1:p.Val335Met
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.982G>A
  hgvsp: ENSP00000445701.1:p.Val328Met
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2225G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1126G>A
  hgvsp: ENSP00000327246.4:p.Val376Met
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*625G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.496G>A
  hgvsp: ENSP00000415371.2:p.Val166Met
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4665
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2989
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val376Met
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

3-42576582-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576582
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576582
    reference: chr 3
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*882G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1003G>T
  hgvsp: ENSP00000394950.1:p.Val335Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.496G>T
  hgvsp: ENSP00000415371.2:p.Val166Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*625G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1126G>T
  hgvsp: ENSP00000327246.4:p.Val376Leu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2225G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.982G>T
  hgvsp: ENSP00000445701.1:p.Val328Leu
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2989
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val376Leu
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

3-42576585-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576585
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576585
    reference: chr 3
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.985G>A
  hgvsp: ENSP00000445701.1:p.Gly329Arg
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.499G>A
  hgvsp: ENSP00000415371.2:p.Gly167Arg
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*885G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1129G>A
  hgvsp: ENSP00000327246.4:p.Gly377Arg
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1006G>A
  hgvsp: ENSP00000394950.1:p.Gly336Arg
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*628G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2228G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4368
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly377Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

3-42576586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576586
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576586
    reference: chr 3
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2229G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*629G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1130G>A
  hgvsp: ENSP00000327246.4:p.Gly377Glu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.986G>A
  hgvsp: ENSP00000445701.1:p.Gly329Glu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*886G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1007G>A
  hgvsp: ENSP00000394950.1:p.Gly336Glu
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.500G>A
  hgvsp: ENSP00000415371.2:p.Gly167Glu
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10502
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4286
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4368
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly377Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

3-42576587-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576587
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576587
    reference: chr 3
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.987G>A
  hgvsp: ENST00000543411.1:c.987G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1008G>A
  hgvsp: ENST00000433647.1:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2230G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.501G>A
  hgvsp: ENST00000438259.2:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1131G>A
  hgvsp: ENST00000325123.4:c.1131G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*630G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*887G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10513
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2987
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly377Gly
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD

3-42576590-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576590
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576590
    reference: chr 3
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1134T>C
  hgvsp: ENST00000325123.4:c.1134T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.990T>C
  hgvsp: ENST00000543411.1:c.990T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1011T>C
  hgvsp: ENST00000433647.1:c.1011T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*890T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2233T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*633T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.504T>C
  hgvsp: ENST00000438259.2:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4365
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4072
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26879
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4282
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser378Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum

3-42576604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576604
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576604
    reference: chr 3
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.510+8C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1017+8C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.996+8C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*639+8C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*896+8C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2239+8C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1140+8C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4072
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
hgvs: c.1140+8C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/3-42576610-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576610
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576610
    reference: chr 3
allele count: 4
allele frequency: 3.297826732183491e-5
allele num: 121292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1017+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*639+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.510+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.996+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2239+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1140+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*896+14A>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9684
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4274
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4622
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

3-42576617-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576617
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576617
    reference: chr 3
allele count: 5
allele frequency: 4.122895261968765e-5
allele num: 121274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*639+21G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.996+21G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*896+21G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1140+21G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1017+21G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.510+21G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2239+21G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9614
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4584
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
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genotype quality: GenotypeQuality
  all individuals: 4070
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genotype quality: GenotypeQuality
  all individuals: 4268
  bin: 8.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 26885
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 7
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genotype quality: GenotypeQuality
  all individuals: 51
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genotype quality: GenotypeQuality
  all individuals: 4351
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

3-42576617-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576617
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576617
    reference: chr 3
allele count: 2
allele frequency: 1.649158104787506e-5
allele num: 121274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.996+21G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.510+21G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*639+21G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*896+21G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1140+21G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2239+21G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1017+21G>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9614
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9798
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26885
  bin: 9.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 4268
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-42576634-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576634
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576634
    reference: chr 3
allele count: 1104
allele frequency: 9.116282142326303e-3
allele num: 121102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.510+38C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.996+38C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2239+38C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1140+38C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*896+38C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1017+38C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*639+38C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 2.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9077
  bin: 2.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 9.75e1
  variant carriers: 766
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 10512
  bin: 3.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 6.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2866
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 49
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

3-42576641-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576641
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576641
    reference: chr 3
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.996+45G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*896+45G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1140+45G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2239+45G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.510+45G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*639+45G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1017+45G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7735
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27337
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

3-42576784-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576784
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576784
    reference: chr 3
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-51T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-51T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-51T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-51T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-51T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-51T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-51T>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22969
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54934
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD

3-42576786-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576786
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576786
    reference: chr 3
allele count: 27
allele frequency: 2.224712435318546e-4
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-49G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-49G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-49G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-49G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-49G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-49G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-49G>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22969
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

3-42576788-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576788
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576788
    reference: chr 3
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-47G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-47G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-47G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-47G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-47G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-47G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-47G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22957
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54925
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

3-42576795-GGTCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576795
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576791
    reference: chr 3
allele count: 9
allele frequency: 7.414730598121601e-5
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-35_2240-32delGTCT
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-35_997-32delGTCT
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-35_1018-32delGTCT
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-35_*640-32delGTCT
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-35_511-32delGTCT
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-35_*897-32delGTCT
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-35_1141-32delGTCT
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22957
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: GGTCT
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

3-42576796-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576796
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576796
    reference: chr 3
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-39G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-39G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-39G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-39G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-39G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-39G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-39G>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22948
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54915
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS

3-42576799-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576799
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576799
    reference: chr 3
allele count: 12
allele frequency: 9.886470365305081e-5
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-36T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-36T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-36T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-36T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-36T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-36T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-36T>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22953
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

3-42576802-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576802
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576802
    reference: chr 3
allele count: 3
allele frequency: 2.47161759132627e-5
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-33C>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-33C>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-33C>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-33C>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-33C>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-33C>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-33C>G
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4450
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22949
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54924
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

3-42576804-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576804
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576804
    reference: chr 3
allele count: 2
allele frequency: 1.647690761397901e-5
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-31A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-31A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-31A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-31A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-31A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-31A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-31A>G
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22946
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
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genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

3-42576806-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576806
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576806
    reference: chr 3
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-29C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-29C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-29C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-29C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-29C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-29C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-29C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22946
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1834
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

3-42576819-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576819
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576819
    reference: chr 3
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-16T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-16T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-16T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-16T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-16T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-16T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-16T>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 9.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
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genotype depth: GenotypeDepth
  all individuals: 814
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22946
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 705
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1898
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

3-42576823-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576823
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576823
    reference: chr 3
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-12C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-12C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-12C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-12C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-12C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-12C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-12C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22947
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54926
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

3-42576833-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576833
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576833
    reference: chr 3
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-2A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-2A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-2A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-2A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-2A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-2A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-2A>G
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22946
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1920
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: c.1141-2A>G
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

3-42576834-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576834
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576834
    reference: chr 3
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.511-1G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1018-1G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.997-1G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2240-1G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*897-1G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*640-1G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1141-1G>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  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: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22944
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1920
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54926
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 9.25e1
  variant carriers: 0
hgvs: c.1141-1G>C
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

3-42576836-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576836
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576836
    reference: chr 3
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1142G>A
  hgvsp: ENSP00000327246.4:p.Gly381Asp
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2241G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.998G>A
  hgvsp: ENSP00000445701.1:p.Gly333Asp
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*898G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.512G>A
  hgvsp: ENSP00000415371.2:p.Gly171Asp
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1019G>A
  hgvsp: ENSP00000394950.1:p.Gly340Asp
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*641G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly381Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

3-42576836-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576836
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576836
    reference: chr 3
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2241G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1142G>C
  hgvsp: ENSP00000327246.4:p.Gly381Ala
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*898G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.998G>C
  hgvsp: ENSP00000445701.1:p.Gly333Ala
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*641G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.512G>C
  hgvsp: ENSP00000415371.2:p.Gly171Ala
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1019G>C
  hgvsp: ENSP00000394950.1:p.Gly340Ala
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22944
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly381Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

3-42576849-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576849
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576849
    reference: chr 3
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1032T>C
  hgvsp: ENST00000433647.1:c.1032T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1011T>C
  hgvsp: ENST00000543411.1:c.1011T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*911T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1155T>C
  hgvsp: ENST00000325123.4:c.1155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2254T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*654T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.525T>C
  hgvsp: ENST00000438259.2:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22943
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54926
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala385Ala
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: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

3-42576869-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576869
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576869
    reference: chr 3
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*674A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2274A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1175A>G
  hgvsp: ENSP00000327246.4:p.Asn392Ser
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1052A>G
  hgvsp: ENSP00000394950.1:p.Asn351Ser
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1031A>G
  hgvsp: ENSP00000445701.1:p.Asn344Ser
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*931A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.545A>G
  hgvsp: ENSP00000415371.2:p.Asn182Ser
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22943
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1921
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn392Ser
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-42576880-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576880
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576880
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1182+4A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*938+4A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1059+4A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.552+4A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*681+4A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2281+4A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1038+4A>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22940
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1182+4A>T
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

3-42576885-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576885
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576885
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.552+9C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1038+9C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*938+9C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1059+9C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2281+9C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*681+9C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1182+9C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22940
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1907
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-42576886-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576886
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576886
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1038+10T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1182+10T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.552+10T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*681+10T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*938+10T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2281+10T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1059+10T>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22939
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

3-42576887-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576887
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576887
    reference: chr 3
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.552+11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1038+11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1182+11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*681+11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1059+11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2281+11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*938+11C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22939
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/3-42576890-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576890
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576890
    reference: chr 3
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*938+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.552+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2281+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1182+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*681+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1038+14A>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1059+14A>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22939
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

3-42576890-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576890
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576890
    reference: chr 3
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2281+14A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.552+14A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*681+14A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*938+14A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1038+14A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1182+14A>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1059+14A>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22939
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

3-42576899-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576899
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576899
    reference: chr 3
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*681+23G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1182+23G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2281+23G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1038+23G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1059+23G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*938+23G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.552+23G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22938
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

3-42576905-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576905
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576905
    reference: chr 3
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1182+29G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.552+29G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*938+29G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*681+29G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2281+29G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1059+29G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1038+29G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22938
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

3-42576922-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576922
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576922
    reference: chr 3
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1038+46G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*681+46G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2281+46G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*938+46G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1182+46G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.552+46G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1059+46G>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22937
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54914
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

3-42576928-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42576928
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42576928
    reference: chr 3
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2281+52G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1059+52G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*938+52G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.552+52G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*681+52G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1182+52G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1038+52G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22937
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54916
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

3-42577534-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577534
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577534
    reference: chr 3
allele count: 2
allele frequency: 9.78760888714887e-5
allele num: 20434
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*939-48T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1039-48T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2282-48T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.553-48T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*682-48T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1060-48T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1183-48T>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20518
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28651
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15017
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2785
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2217
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2653
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9601
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD

3-42577544-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577544
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577544
    reference: chr 3
allele count: 1
allele frequency: 4.686474833630143e-5
allele num: 21338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*939-38T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1039-38T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2282-38T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1183-38T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.553-38T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*682-38T>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1060-38T>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7181
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21815
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2923
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5306
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

3-42577548-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577548
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577548
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 21864
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*682-34C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.553-34C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*939-34C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1183-34C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2282-34C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1039-34C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1060-34C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 30891
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17749
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14733
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24417
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2245
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

3-42577565-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577565
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577565
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 28816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*939-17A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1060-17A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*682-17A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.553-17A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1039-17A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2282-17A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1183-17A>G
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10397
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7987
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35152
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3132
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2766
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32927
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2117
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4460
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

3-42577571-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577571
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577571
    reference: chr 3
allele count: 4
allele frequency: 1.265342275085411e-4
allele num: 31612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.553-11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1060-11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*682-11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2282-11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1039-11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1183-11C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*939-11C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8519
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35587
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7912
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
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  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1940
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 992
  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

3-42577572-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577572
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577572
    reference: chr 3
allele count: 5
allele frequency: 1.548371113588505e-4
allele num: 32292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1060-10C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*939-10C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*682-10C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1183-10C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1039-10C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2282-10C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.553-10C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35547
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5906
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1889
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2986
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7827
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-42577577-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577577
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577577
    reference: chr 3
allele count: 889
allele frequency: 2.44876597620097e-2
allele num: 36304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1039-5C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1183-5C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1060-5C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.553-5C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*682-5C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2282-5C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*939-5C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 2.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6538
  bin: 2.25e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 1.25e1
  variant carriers: 434
genotype depth: GenotypeDepth
  all individuals: 34892
  bin: 7.5e0
  variant carriers: 268
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 1.75e1
  variant carriers: 271
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 2.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 33834
  bin: 2.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2763
  bin: 2.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 1.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 6646
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 8.25e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 4.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 3.75e1
  variant carriers: 6
hgvs: c.1183-5C>T
num of homozygotes: 6
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

3-42577581-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577581
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577581
    reference: chr 3
allele count: 1
allele frequency: 2.569769234722722e-5
allele num: 38914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.553-1G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2282-1G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1060-1G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1039-1G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*682-1G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1183-1G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*939-1G>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7602
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33836
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6062
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1703
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1183-1G>T
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

3-42577584-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577584
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577584
    reference: chr 3
allele count: 88
allele frequency: 2.144458524222634e-3
allele num: 41036
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1185G>A
  hgvsp: ENST00000325123.4:c.1185G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*684G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*941G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1041G>A
  hgvsp: ENST00000543411.1:c.1041G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1062G>A
  hgvsp: ENST00000433647.1:c.1062G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.555G>A
  hgvsp: ENST00000438259.2:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2284G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7626
  bin: 1.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33867
  bin: 7.5e0
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 8863
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2701
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9417
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5644
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1185G>A
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP

3-42577586-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577586
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577586
    reference: chr 3
allele count: 1
allele frequency: 2.31878681074062e-5
allele num: 43126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1064A>G
  hgvsp: ENSP00000394950.1:p.Gln355Arg
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*943A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*686A>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.557A>G
  hgvsp: ENSP00000415371.2:p.Gln186Arg
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1187A>G
  hgvsp: ENSP00000327246.4:p.Gln396Arg
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1043A>G
  hgvsp: ENSP00000445701.1:p.Gln348Arg
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2286A>G
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7535
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5328
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2639
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33528
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Gln396Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-42577588-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577588
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577588
    reference: chr 3
allele count: 1
allele frequency: 2.238538681948424e-5
allele num: 44672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2288G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*688G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1045G>A
  hgvsp: ENSP00000445701.1:p.Ala349Thr
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1189G>A
  hgvsp: ENSP00000327246.4:p.Ala397Thr
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1066G>A
  hgvsp: ENSP00000394950.1:p.Ala356Thr
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.559G>A
  hgvsp: ENSP00000415371.2:p.Ala187Thr
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*945G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32779
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2247
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala397Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

3-42577593-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577593
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577593
    reference: chr 3
allele count: 128
allele frequency: 2.604166666666667e-3
allele num: 49152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1050G>A
  hgvsp: ENST00000543411.1:c.1050G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.564G>A
  hgvsp: ENST00000438259.2:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1194G>A
  hgvsp: ENST00000325123.4:c.1194G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1071G>A
  hgvsp: ENST00000433647.1:c.1071G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*693G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*950G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2293G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 1.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 2.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 1.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31106
  bin: 7.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 9.75e1
  variant carriers: 125
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2455
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu398Glu
num of homozygotes: 1
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

3-42577594-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577594
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577594
    reference: chr 3
allele count: 1
allele frequency: 2.013206635529071e-5
allele num: 49672
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*951C>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.565C>G
  hgvsp: ENSP00000415371.2:p.Leu189Val
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*694C>G
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1072C>G
  hgvsp: ENSP00000394950.1:p.Leu358Val
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1051C>G
  hgvsp: ENSP00000445701.1:p.Leu351Val
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1195C>G
  hgvsp: ENSP00000327246.4:p.Leu399Val
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2294C>G
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7288
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2466
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31959
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4694
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu399Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

3-42577596-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577596
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577596
    reference: chr 3
allele count: 1
allele frequency: 1.96479094624332e-5
allele num: 50896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.567G>C
  hgvsp: ENST00000438259.2:c.567G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*953G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1197G>C
  hgvsp: ENST00000325123.4:c.1197G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1074G>C
  hgvsp: ENST00000433647.1:c.1074G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*696G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2296G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1053G>C
  hgvsp: ENST00000543411.1:c.1053G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31478
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4700
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu399Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

3-42577599-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577599
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577599
    reference: chr 3
allele count: 3
allele frequency: 6.042782902952906e-5
allele num: 49646
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*956G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1077G>A
  hgvsp: ENST00000433647.1:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.570G>A
  hgvsp: ENST00000438259.2:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*699G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1200G>A
  hgvsp: ENST00000325123.4:c.1200G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1056G>A
  hgvsp: ENST00000543411.1:c.1056G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2299G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8820
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26376
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5252
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg400Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-42577601-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577601
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577601
    reference: chr 3
allele count: 1
allele frequency: 1.953048709034803e-5
allele num: 51202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*701G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1079G>C
  hgvsp: ENSP00000394950.1:p.Arg360Pro
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1058G>C
  hgvsp: ENSP00000445701.1:p.Arg353Pro
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*958G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.572G>C
  hgvsp: ENSP00000415371.2:p.Arg191Pro
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2301G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1202G>C
  hgvsp: ENSP00000327246.4:p.Arg401Pro
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2475
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3331
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1429
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1919
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8823
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg401Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum

3-42577608-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577608
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577608
    reference: chr 3
allele count: 1
allele frequency: 1.863099452248761e-5
allele num: 53674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*708G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.579G>C
  hgvsp: ENSP00000415371.2:p.Trp193Cys
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2308G>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1086G>C
  hgvsp: ENSP00000394950.1:p.Trp362Cys
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1065G>C
  hgvsp: ENSP00000445701.1:p.Trp355Cys
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1209G>C
  hgvsp: ENSP00000327246.4:p.Trp403Cys
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*965G>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9887
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  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 quality: GenotypeQuality
  all individuals: 2438
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2021
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Trp403Cys
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

3-42577620-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577620
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577620
    reference: chr 3
allele count: 1
allele frequency: 1.690674240887266e-5
allele num: 59148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1098C>T
  hgvsp: ENST00000433647.1:c.1098C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2320C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1221C>T
  hgvsp: ENST00000325123.4:c.1221C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.591C>T
  hgvsp: ENST00000438259.2:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*977C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1077C>T
  hgvsp: ENST00000543411.1:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*720C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15889
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2201
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29243
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3788
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His407His
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

3-42577624-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577624
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577624
    reference: chr 3
allele count: 1
allele frequency: 1.65371258475277e-5
allele num: 60470
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1225C>T
  hgvsp: ENSP00000327246.4:p.Gln409Ter
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1081C>T
  hgvsp: ENSP00000445701.1:p.Gln361Ter
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2324C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1102C>T
  hgvsp: ENSP00000394950.1:p.Gln368Ter
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*724C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*981C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.595C>T
  hgvsp: ENSP00000415371.2:p.Gln199Ter
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8039
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 2.75e1
  variant carriers: 0
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: 22
  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: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2025
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17103
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3573
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln409Ter
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

3-42577629-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577629
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577629
    reference: chr 3
allele count: 3
allele frequency: 4.876462938881665e-5
allele num: 61520
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*986C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1107C>T
  hgvsp: ENST00000433647.1:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.600C>T
  hgvsp: ENST00000438259.2:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1230C>T
  hgvsp: ENST00000325123.4:c.1230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1086C>T
  hgvsp: ENST00000543411.1:c.1086C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*729C>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2329C>T
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7939
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26120
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15252
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3218
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17452
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28870
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly410Gly
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

3-42577630-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577630
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577630
    reference: chr 3
allele count: 3
allele frequency: 4.835745833199007e-5
allele num: 62038
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1231G>A
  hgvsp: ENSP00000327246.4:p.Val411Ile
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1087G>A
  hgvsp: ENSP00000445701.1:p.Val363Ile
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*730G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.601G>A
  hgvsp: ENSP00000415371.2:p.Val201Ile
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2330G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*987G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1108G>A
  hgvsp: ENSP00000394950.1:p.Val370Ile
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15573
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17753
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val411Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

3-42577630-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577630
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577630
    reference: chr 3
allele count: 1
allele frequency: 1.611915277733003e-5
allele num: 62038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*987G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1087G>T
  hgvsp: ENSP00000445701.1:p.Val363Phe
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1231G>T
  hgvsp: ENSP00000327246.4:p.Val411Phe
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1108G>T
  hgvsp: ENSP00000394950.1:p.Val370Phe
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*730G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2330G>T
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.601G>T
  hgvsp: ENSP00000415371.2:p.Val201Phe
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.25e1
  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: 79
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3139
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val411Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

3-42577631-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577631
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577631
    reference: chr 3
allele count: 1
allele frequency: 1.6e-5
allele num: 62500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*988T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1109T>C
  hgvsp: ENSP00000394950.1:p.Val370Ala
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2331T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1088T>C
  hgvsp: ENSP00000445701.1:p.Val363Ala
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1232T>C
  hgvsp: ENSP00000327246.4:p.Val411Ala
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*731T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.602T>C
  hgvsp: ENSP00000415371.2:p.Val201Ala
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3042
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17992
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val411Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

3-42577634-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577634
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577634
    reference: chr 3
allele count: 1
allele frequency: 1.571931589537223e-5
allele num: 63616
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1235T>C
  hgvsp: ENSP00000327246.4:p.Leu412Pro
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*734T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1112T>C
  hgvsp: ENSP00000394950.1:p.Leu371Pro
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1091T>C
  hgvsp: ENSP00000445701.1:p.Leu364Pro
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2334T>C
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.605T>C
  hgvsp: ENSP00000415371.2:p.Leu202Pro
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*991T>C
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7640
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19405
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu412Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

3-42577637-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42577637
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 42577637
    reference: chr 3
allele count: 1
allele frequency: 1.549522746993926e-5
allele num: 64536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000394950
  ensembl transcript: ENST00000433647
  gene symbol: VIPR1
  hgvsc: ENST00000433647.1:c.1115G>A
  hgvsp: ENSP00000394950.1:p.Gly372Asp
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000403680
  ensembl transcript: ENST00000439910
  gene symbol: VIPR1
  hgvsc: ENST00000439910.1:c.*737G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000327246
  ensembl transcript: ENST00000325123
  gene symbol: VIPR1
  hgvsc: ENST00000325123.4:c.1238G>A
  hgvsp: ENSP00000327246.4:p.Gly413Asp
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000388479
  ensembl transcript: ENST00000443646
  gene symbol: VIPR1
  hgvsc: ENST00000443646.1:c.*994G>A
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000415371
  ensembl transcript: ENST00000438259
  gene symbol: VIPR1
  hgvsc: ENST00000438259.2:c.608G>A
  hgvsp: ENSP00000415371.2:p.Gly203Asp
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114812
  ensembl protein: ENSP00000445701
  ensembl transcript: ENST00000543411
  gene symbol: VIPR1
  hgvsc: ENST00000543411.1:c.1094G>A
  hgvsp: ENSP00000445701.1:p.Gly365Asp
  variant of: http://identifiers.org/hgnc/12694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114812
  ensembl transcript: ENST00000498102
  gene symbol: VIPR1
  hgvsc: ENST00000498102.1:n.2337G>A
  variant of: http://identifiers.org/hgnc/12694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7532
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly413Asp
num of homozygotes: 0
reference allele: G

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

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4287
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2998
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4668
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10618
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4073
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2813
bin: 8.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 4
allele frequency: 3.843936190659235e-4
allele num: 10406
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.52e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.374894e6

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.17e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 2.039e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 7.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
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SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 4.255e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.96e-1

BaseQRankSum
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SIO_000300: 5.56e0

DP
type: SiteQuality
SIO_000300: 2.374828e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.67e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.392e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 14

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 13
allele frequency: 1.948149258204705e-4
allele num: 66730
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.37e-1

VQSLOD
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ClippingRankSum
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SIO_000300: -1.86e-1

ReadPosRankSum
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SIO_000300: 7.04e-1

MQRankSum
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DP
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SIO_000300: 2.376483e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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SIO_000300: 1.192e1

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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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 6.858e0

InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: -2.424e-1

ReadPosRankSum
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SIO_000300: -4.9e-2

ClippingRankSum
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SIO_000300: 4.25e-1

DP
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SIO_000300: 2.376347e6

QD
type: SiteQuality
SIO_000300: 9.9e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.436e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.158e0

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.334e0

VQSLOD
type: SiteQuality
SIO_000300: 6.03e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

DP
type: SiteQuality
SIO_000300: 2.375926e6

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.225e0

QD
type: SiteQuality
SIO_000300: 1.57e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.83e0

FS
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.955e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.49e-1

DP
type: SiteQuality
SIO_000300: 2.375893e6

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

QD
type: SiteQuality
SIO_000300: 1.057e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.996282304970918e-5
allele num: 66708
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.56e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.376384e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
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allele num: 16512
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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Other
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FS
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QD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
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SIO_000300: 5.967e1

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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variant carriers: 0

East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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MQ
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MQRankSum
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FS
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InbreedingCoeff
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DP
type: SiteQuality
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BaseQRankSum
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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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African
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num of homozygotes: 0

South Asian
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Other
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num of homozygotes: 0

East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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DP
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FS
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQ
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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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variant carriers: 0

Other
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

DP
type: SiteQuality
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ReadPosRankSum
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FS
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BaseQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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SIO_000300: -2.0e-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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bin: 6.75e1
variant carriers: 0

South Asian
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allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

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

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

InbreedingCoeff
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DP
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VQSLOD
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MQ
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FS
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SIO_000300: 1.034e0

MQRankSum
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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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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variant carriers: 1

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

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

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

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

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

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

Other
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.089e0

MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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SIO_000300: -1.691e0

VQSLOD
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DP
type: SiteQuality
SIO_000300: 2.376102e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.75e-1

QD
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SIO_000300: 8.15e0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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ReadPosRankSum
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SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 3.154e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.72e0

DP
type: SiteQuality
SIO_000300: 2.376113e6

QD
type: SiteQuality
SIO_000300: 1.583e1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
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bin: 8.75e1
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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -3.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e-1

FS
type: SiteQuality
SIO_000300: 1.214e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.13e-1

BaseQRankSum
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SIO_000300: -4.382e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.49e-1

QD
type: SiteQuality
SIO_000300: 1.075e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

DP
type: SiteQuality
SIO_000300: 2.374438e6

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

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

Other
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allele num: 908
num of homozygotes: 0

South Asian
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allele count: 4
allele frequency: 2.429838415745353e-4
allele num: 16462
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
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FS
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SIO_000300: 0.0e0

QD
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BaseQRankSum
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ClippingRankSum
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DP
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.000780101413184e-5
allele num: 66658
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

FS
type: SiteQuality
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DP
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
type: Population
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

Other
type: Population
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allele num: 908
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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66658
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European (Finnish)
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South Asian
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DP
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SIO_000300: 2.370207e6

VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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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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Other
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allele num: 906
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East Asian
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European (Non-Finnish)
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allele num: 66618
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African
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allele frequency: 9.118891881492881e-2
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European (Finnish)
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Latino
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allele frequency: 9.414406633269996e-3
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
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East Asian
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European (Finnish)
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ClippingRankSum
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MQ
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FS
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DP
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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SIO_000300: 1.569e1

VQSLOD
type: SiteQuality
SIO_000300: 7.9e-2

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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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.71e-1

DP
type: SiteQuality
SIO_000300: 5.32909e6

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 4.555e0

QD
type: SiteQuality
SIO_000300: 1.214e1

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

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

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

South Asian
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allele count: 25
allele frequency: 1.515886490419597e-3
allele num: 16492
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

VQSLOD
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QD
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SIO_000300: 1.384e1

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.62e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-1

FS
type: SiteQuality
SIO_000300: 2.898e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

DP
type: SiteQuality
SIO_000300: 5.328996e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.68e-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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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.327e0

DP
type: SiteQuality
SIO_000300: 5.327452e6

MQRankSum
type: SiteQuality
SIO_000300: 7.19e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.763e0

FS
type: SiteQuality
SIO_000300: 5.656e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.349001738713352e-4
allele num: 66716
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.053e0

VQSLOD
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SIO_000300: 4.07e0

MQ
type: SiteQuality
SIO_000300: 5.811e1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.182e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.22e-1

DP
type: SiteQuality
SIO_000300: 5.328623e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 5.326532e6

QD
type: SiteQuality
SIO_000300: 1.283e1

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.442e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.453e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.37e-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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variant carriers: 12

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 12
allele frequency: 1.798830760005996e-4
allele num: 66710
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 5.328871e6

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

FS
type: SiteQuality
SIO_000300: 5.44e-1

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.953e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.120000000000001e-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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variant carriers: 0

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

East Asian
type: Population
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.49667246237784e-5
allele num: 66716
num of homozygotes: 0

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

South Asian
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allele num: 16502
num of homozygotes: 0

InbreedingCoeff
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VQSLOD
type: SiteQuality
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BaseQRankSum
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DP
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MQ
type: SiteQuality
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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QD
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SIO_000300: 1.311e1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

East Asian
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.336e1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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BaseQRankSum
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-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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variant carriers: 0

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

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

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

ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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FS
type: SiteQuality
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BaseQRankSum
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DP
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QD
type: SiteQuality
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VQSLOD
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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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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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African
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allele num: 10406
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Latino
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South Asian
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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South Asian
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Latino
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European (Finnish)
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Other
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FS
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BaseQRankSum
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DP
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MQ
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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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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South Asian
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Latino
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East 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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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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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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South Asian
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Latino
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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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Other
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MQ
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MQRankSum
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QD
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InbreedingCoeff
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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Latino
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East Asian
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Other
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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QD
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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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European (Non-Finnish)
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European (Finnish)
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Latino
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African
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South Asian
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East Asian
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Other
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQ
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FS
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DP
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QD
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VQSLOD
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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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European (Finnish)
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European (Non-Finnish)
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Other
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Latino
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African
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East Asian
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South Asian
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DP
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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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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African
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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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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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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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South Asian
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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DP
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MQRankSum
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FS
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MQ
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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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African
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East Asian
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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FS
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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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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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.18e-1

ReadPosRankSum
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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SIO_000300: -1.352e0

QD
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VQSLOD
type: SiteQuality
SIO_000300: 5.79e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
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SIO_000300: 0.0e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

MQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 5.86e-1

DP
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SIO_000300: 5.325645e6

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
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

ClippingRankSum
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SIO_000300: -5.6e-2

BaseQRankSum
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FS
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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QD
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SIO_000300: 1.081e1

VQSLOD
type: SiteQuality
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DP
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SIO_000300: 5.325436e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
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allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 6.96e-1

MQ
type: SiteQuality
SIO_000300: 5.885e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

BaseQRankSum
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SIO_000300: -5.728e0

DP
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SIO_000300: 5.325436e6

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -6.949e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

QD
type: SiteQuality
SIO_000300: 1.081e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.324598e6

QD
type: SiteQuality
SIO_000300: 4.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.423e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 910
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GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
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South Asian
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allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 0.0e0

FS
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SIO_000300: 1.561e0

ReadPosRankSum
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BaseQRankSum
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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VQSLOD
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.324154e6

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

BaseQRankSum
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MQRankSum
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MQ
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FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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QD
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InbreedingCoeff
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

FS
type: SiteQuality
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DP
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ClippingRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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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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variant carriers: 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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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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allele count: 2
allele frequency: 1.868460388639761e-4
allele num: 10704
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

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

BaseQRankSum
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DP
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MQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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VQSLOD
type: SiteQuality
SIO_000300: -1.574e0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4197
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5005
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2696
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1414
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.03e-2

QD
type: SiteQuality
SIO_000300: 1.141e1

DP
type: SiteQuality
SIO_000300: 4.5798e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

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

GenotypeQuality
all individuals: 1028
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9612
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 9.25e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5660
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2072
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14798
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.41716e5

QD
type: SiteQuality
SIO_000300: 1.012e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.07e-2

FS
type: SiteQuality
SIO_000300: 4.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.414e0

GenotypeQuality
all individuals: 523
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1455
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5698
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33979
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 142
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 1.39178844815588e-3
allele num: 2874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6158
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.86e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.093e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 5.74017e5

QD
type: SiteQuality
SIO_000300: 8.33e0

GenotypeQuality
all individuals: 34073
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1367
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 293
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 125
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2630
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 1.706484641638225e-3
allele num: 2930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.16e0

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

DP
type: SiteQuality
SIO_000300: 5.80078e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.083e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.81e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

GenotypeQuality
all individuals: 310
bin: 5.25e1
variant carriers: 19

GenotypeQuality
all individuals: 594
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 894
bin: 9.75e1
variant carriers: 845

GenotypeQuality
all individuals: 1525
bin: 1.75e1
variant carriers: 10

GenotypeQuality
all individuals: 172
bin: 5.75e1
variant carriers: 14

GenotypeQuality
all individuals: 167
bin: 7.75e1
variant carriers: 36

GenotypeQuality
all individuals: 2418
bin: 3.25e1
variant carriers: 11

GenotypeQuality
all individuals: 55
bin: 8.75e1
variant carriers: 40

GenotypeQuality
all individuals: 7306
bin: 6.25e1
variant carriers: 23

GenotypeQuality
all individuals: 160
bin: 7.25e1
variant carriers: 16

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 40

GenotypeQuality
all individuals: 732
bin: 6.75e1
variant carriers: 29

Other
type: Population
allele count: 4
allele frequency: 1.526717557251908e-2
allele num: 262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 720
allele frequency: 3.792267986937744e-2
allele num: 18986
num of homozygotes: 5

European (Finnish)
type: Population
allele count: 52
allele frequency: 5.752212389380531e-2
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 43
allele frequency: 1.292844257366206e-2
allele num: 3326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2642
num of homozygotes: 0

African
type: Population
allele count: 50
allele frequency: 1.484560570071259e-2
allele num: 3368
num of homozygotes: 1

South Asian
type: Population
allele count: 20
allele frequency: 2.934272300469483e-3
allele num: 6816
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.246e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.299e0

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.16338e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
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variant carriers: 0

GenotypeQuality
all individuals: 8510
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 2735
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variant carriers: 0

GenotypeQuality
all individuals: 922
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variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 2.885170225043277e-4
allele num: 3466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 982
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.02e0

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

MQ
type: SiteQuality
SIO_000300: 5.739e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.47e-2

FS
type: SiteQuality
SIO_000300: 2.093e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.253e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.614e0

DP
type: SiteQuality
SIO_000300: 6.38516e5

GenotypeQuality
all individuals: 391
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1435
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33718
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 292
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 2345
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variant carriers: 0

GenotypeQuality
all individuals: 841
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GenotypeQuality
all individuals: 130
bin: 9.75e1
variant carriers: 88

GenotypeQuality
all individuals: 391
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variant carriers: 1

GenotypeQuality
all individuals: 959
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variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 8.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3034
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1046
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 1.298026998961578e-3
allele num: 3852
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 3.378378378378379e-3
allele num: 296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7522
num of homozygotes: 0

African
type: Population
allele count: 82
allele frequency: 2.225841476655809e-2
allele num: 3684
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21602
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.466e0

QD
type: SiteQuality
SIO_000300: 1.245e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

FS
type: SiteQuality
SIO_000300: 1.166e0

DP
type: SiteQuality
SIO_000300: 6.56606e5

GenotypeQuality
all individuals: 10637
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 974
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 5.75e1
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GenotypeQuality
all individuals: 2254
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
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variant carriers: 0

GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 197
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variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.391743522178305e-5
allele num: 22770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1094
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.75709e5

VQSLOD
type: SiteQuality
SIO_000300: 1.09e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

QD
type: SiteQuality
SIO_000300: 8.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.133e0

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

GenotypeQuality
all individuals: 5128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2609
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
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variant carriers: 0

GenotypeQuality
all individuals: 33084
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variant carriers: 0

GenotypeQuality
all individuals: 161
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GenotypeQuality
all individuals: 213
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GenotypeQuality
all individuals: 996
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GenotypeQuality
all individuals: 42
bin: 9.75e1
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GenotypeQuality
all individuals: 10971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.22225975342003e-5
allele num: 23684
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7988
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4326
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.224e0

FS
type: SiteQuality
SIO_000300: 4.365e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

DP
type: SiteQuality
SIO_000300: 6.86584e5

GenotypeQuality
all individuals: 4733
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 250
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2194
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 991
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32010
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 13040
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 180
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 259
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 306
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 387
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 5

Latino
type: Population
allele count: 11
allele frequency: 2.285002077274616e-3
allele num: 4814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1268
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3724
num of homozygotes: 0

African
type: Population
allele count: 116
allele frequency: 2.707749766573296e-2
allele num: 4284
num of homozygotes: 1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.134e0

QD
type: SiteQuality
SIO_000300: 1.237e1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.87e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.38e-1

DP
type: SiteQuality
SIO_000300: 7.2651e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
all individuals: 13239
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 81
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1284
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4280
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.17e-2

DP
type: SiteQuality
SIO_000300: 7.30993e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.067e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.52e1

MQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.066e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.680800942285041e-5
allele num: 27168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8864
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

QD
type: SiteQuality
SIO_000300: 7.12e0

DP
type: SiteQuality
SIO_000300: 7.39885e5

GenotypeQuality
all individuals: 4610
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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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 101
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GenotypeQuality
all individuals: 1969
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4060
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.135847342117219e-4
allele num: 26412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3754
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4974
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8924
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.747e0

DP
type: SiteQuality
SIO_000300: 7.45927e5

MQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

QD
type: SiteQuality
SIO_000300: 8.35e0

VQSLOD
type: SiteQuality
SIO_000300: -4.21e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.37e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
all individuals: 601
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
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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
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 2061
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5094
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9122
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.367424242424242e-4
allele num: 4224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.098e0

MQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

DP
type: SiteQuality
SIO_000300: 7.49121e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

GenotypeQuality
all individuals: 943
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variant carriers: 0

GenotypeQuality
all individuals: 249
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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
all individuals: 11171
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GenotypeQuality
all individuals: 47
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28666
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1416
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.477700693756194e-4
allele num: 4036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.55051e5

BaseQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.22e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.033e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-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
all individuals: 496
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5910
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.120441051738762e-4
allele num: 4716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1580
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31768
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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FS
type: SiteQuality
SIO_000300: 2.906e0

MQ
type: SiteQuality
SIO_000300: 5.684e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.02e-2

MQRankSum
type: SiteQuality
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QD
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SIO_000300: 1.758e1

DP
type: SiteQuality
SIO_000300: 7.92915e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.575e-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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.070310101320233e-5
allele num: 32570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6026
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

DP
type: SiteQuality
SIO_000300: 8.08054e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

VQSLOD
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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4878
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 3
allele frequency: 6.504770164787511e-4
allele num: 4612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6128
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.1e-1

FS
type: SiteQuality
SIO_000300: 3.27e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.2012e5

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

QD
type: SiteQuality
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ReadPosRankSum
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
all individuals: 224
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4664
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 3.254149040026033e-4
allele num: 6146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.982225933436717e-5
allele num: 33532
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-1

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.914e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -2.541e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.24049e5

GenotypeQuality
all individuals: 2005
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28896
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17753
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10626
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.144082332761578e-4
allele num: 4664
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4912
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.98e-1

DP
type: SiteQuality
SIO_000300: 8.24049e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

MQ
type: SiteQuality
SIO_000300: 5.914e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.541e-1

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-1

GenotypeQuality
all individuals: 896
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28783
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 393
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1794
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33770
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10660
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4974
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4702
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.60926939169617e-4
allele num: 6214
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.26297e5

MQ
type: SiteQuality
SIO_000300: 5.896e1

FS
type: SiteQuality
SIO_000300: 1.957e0

VQSLOD
type: SiteQuality
SIO_000300: -5.780999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.111e0

QD
type: SiteQuality
SIO_000300: 1.159e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
all individuals: 621
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28640
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1892
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.900232018561485e-5
allele num: 34480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4772
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5030
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: -5.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

DP
type: SiteQuality
SIO_000300: 8.40414e5