1-231906798-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906798
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906798
    reference: chr 1
allele count: 1
allele frequency: 1.495394185907405e-5
allele num: 66872
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1746C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1616C>T
  hgvsp: ENSP00000295051.7:p.Pro539Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1477C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1746C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1616C>T
  hgvsp: ENSP00000440909.1:p.Pro539Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1616C>T
  hgvsp: ENSP00000440953.1:p.Pro539Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*475C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1616C>T
  hgvsp: ENSP00000441193.1:p.Pro539Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1616C>T
  hgvsp: ENSP00000403888.2:p.Pro539Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1616C>T
  hgvsp: ENSP00000355596.4:p.Pro539Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1616C>T
  hgvsp: ENSP00000443996.1:p.Pro539Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-389C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1616C>T
  hgvsp: ENSP00000473425.1:p.Pro539Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1477C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1675C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1762C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.566C>T
  hgvsp: ENSP00000473386.1:p.Pro189Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*316C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*475C>T
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro539Leu
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

1-231906798-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906798
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906798
    reference: chr 1
allele count: 1
allele frequency: 1.495394185907405e-5
allele num: 66872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*475C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1762C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*316C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*475C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-389C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*475C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.566C>G
  hgvsp: ENSP00000473386.1:p.Pro189Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1616C>G
  hgvsp: ENSP00000440953.1:p.Pro539Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1616C>G
  hgvsp: ENSP00000295051.7:p.Pro539Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1616C>G
  hgvsp: ENSP00000355596.4:p.Pro539Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1616C>G
  hgvsp: ENSP00000403888.2:p.Pro539Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1746C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1616C>G
  hgvsp: ENSP00000443996.1:p.Pro539Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1616C>G
  hgvsp: ENSP00000355593.3:p.Pro539Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1616C>G
  hgvsp: ENSP00000441193.1:p.Pro539Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1616C>G
  hgvsp: ENSP00000473425.1:p.Pro539Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1746C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1675C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1477C>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro539Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/1-231906801-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906801
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906801
    reference: chr 1
allele count: 29
allele frequency: 4.437100278466293e-4
allele num: 65358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1619C>A
  hgvsp: ENSP00000295051.7:p.Pro540Gln
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1619C>A
  hgvsp: ENSP00000443996.1:p.Pro540Gln
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1678C>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1619C>A
  hgvsp: ENSP00000473425.1:p.Pro540Gln
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1749C>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1749C>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-386C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1619C>A
  hgvsp: ENSP00000403888.2:p.Pro540Gln
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*478C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.569C>A
  hgvsp: ENSP00000473386.1:p.Pro190Gln
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1480C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*319C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*478C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1480C>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1619C>A
  hgvsp: ENSP00000440909.1:p.Pro540Gln
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1619C>A
  hgvsp: ENSP00000355593.3:p.Pro540Gln
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1619C>A
  hgvsp: ENSP00000440953.1:p.Pro540Gln
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1619C>A
  hgvsp: ENSP00000355596.4:p.Pro540Gln
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1765C>A
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro540Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-231906801-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906801
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906801
    reference: chr 1
allele count: 1
allele frequency: 1.53003457878148e-5
allele num: 65358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*478C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1619C>G
  hgvsp: ENSP00000473425.1:p.Pro540Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1619C>G
  hgvsp: ENSP00000440909.1:p.Pro540Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.569C>G
  hgvsp: ENSP00000473386.1:p.Pro190Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-386C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1765C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1749C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1619C>G
  hgvsp: ENSP00000355596.4:p.Pro540Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*478C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1619C>G
  hgvsp: ENSP00000403888.2:p.Pro540Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1619C>G
  hgvsp: ENSP00000440953.1:p.Pro540Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*319C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1619C>G
  hgvsp: ENSP00000295051.7:p.Pro540Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*478C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1619C>G
  hgvsp: ENSP00000355593.3:p.Pro540Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1619C>G
  hgvsp: ENSP00000443996.1:p.Pro540Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1480C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1619C>G
  hgvsp: ENSP00000441193.1:p.Pro540Arg
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1480C>G
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro540Arg
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

1-231906802-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906802
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906802
    reference: chr 1
allele count: 1
allele frequency: 1.554774713144065e-5
allele num: 64318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1679G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*479G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1620G>A
  hgvsp: ENST00000295051.7:c.1620G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1620G>A
  hgvsp: ENST00000539444.1:c.1620G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1481G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1620G>A
  hgvsp: ENST00000535983.1:c.1620G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*479G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*320G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1620G>A
  hgvsp: ENST00000535944.1:c.1620G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1750G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1620G>A
  hgvsp: ENST00000366633.3:c.1620G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1620G>A
  hgvsp: ENST00000537876.1:c.1620G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1620G>A
  hgvsp: ENST00000602281.1:c.1620G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1750G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1620G>A
  hgvsp: ENST00000439617.2:c.1620G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.570G>A
  hgvsp: ENST00000602873.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1481G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1766G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-385G>A
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro540Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-231906813-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906813
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906813
    reference: chr 1
allele count: 1
allele frequency: 1.782658300057045e-5
allele num: 56096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1690G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1631G>A
  hgvsp: ENSP00000441193.1:p.Arg544Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1492G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1631G>A
  hgvsp: ENSP00000440909.1:p.Arg544Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*490G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*490G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1631G>A
  hgvsp: ENSP00000355596.4:p.Arg544Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1631G>A
  hgvsp: ENSP00000403888.2:p.Arg544Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1631G>A
  hgvsp: ENSP00000443996.1:p.Arg544Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1631G>A
  hgvsp: ENSP00000440953.1:p.Arg544Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1631G>A
  hgvsp: ENSP00000295051.7:p.Arg544Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*331G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1761G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.581G>A
  hgvsp: ENSP00000473386.1:p.Arg194Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-374G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1761G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1777G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*490G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1631G>A
  hgvsp: ENSP00000355593.3:p.Arg544Lys
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg544Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-231906816-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906816
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906816
    reference: chr 1
allele count: 1
allele frequency: 1.875328182431926e-5
allele num: 53324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634G>A
  hgvsp: ENSP00000443996.1:p.Ser545Asn
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634G>A
  hgvsp: ENSP00000473425.1:p.Ser545Asn
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634G>A
  hgvsp: ENSP00000295051.7:p.Arg545Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634G>A
  hgvsp: ENSP00000403888.2:p.Ser545Asn
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634G>A
  hgvsp: ENSP00000440953.1:p.Ser545Asn
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1634G>A
  hgvsp: ENSP00000441193.1:p.Arg545Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584G>A
  hgvsp: ENSP00000473386.1:p.Arg195Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634G>A
  hgvsp: ENSP00000355596.4:p.Ser545Asn
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634G>A
  hgvsp: ENSP00000440909.1:p.Arg545Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634G>A
  hgvsp: ENSP00000355593.3:p.Ser545Asn
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493G>A
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser545Asn
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-231906823-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906823
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906823
    reference: chr 1
allele count: 15
allele frequency: 3.172052106242599e-4
allele num: 47288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+7C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+7C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+7C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+7C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1634+7C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+7C>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1634+7C>G
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-231906829-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906829
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906829
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 42270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+13T>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+13T>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+13T>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+13T>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+13T>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1634+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+13T>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+13T>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

1-231906836-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906836
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906836
    reference: chr 1
allele count: 1
allele frequency: 2.793296089385475e-5
allele num: 35800
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+20T>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1634+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+20T>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+20T>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+20T>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+20T>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+20T>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+20T>A
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-231906845-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906845
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906845
    reference: chr 1
allele count: 1
allele frequency: 3.627394080092861e-5
allele num: 27568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+29G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+29G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+29G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+29G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1634+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+29G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+29G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+29G>A
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

1-231906847-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906847
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906847
    reference: chr 1
allele count: 2372
allele frequency: 9.057583626088285e-2
allele num: 26188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1634+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+31C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+31C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+31C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+31C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+31C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+31C>T
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 143
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

1-231906848-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906848
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906848
    reference: chr 1
allele count: 1
allele frequency: 4.184450581638631e-5
allele num: 23898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+32G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+32G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+32G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+32G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+32G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+32G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+32G>A
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

1-231906851-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231906851
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231906851
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 21824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+35C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+35C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+35C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+35C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+35C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1634+35C>T
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

1-231910381-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910381
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910381
    reference: chr 1
allele count: 1
allele frequency: 1.506931886678722e-4
allele num: 6636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3565G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1635-4G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3565G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3565G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3565G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3565G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3565G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+3565G>T
  variant of: http://identifiers.org/hgnc/2888
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1635-4G>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

1-231910382-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910382
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910382
    reference: chr 1
allele count: 1
allele frequency: 1.453488372093023e-4
allele num: 6880
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3566T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1635-3T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3566T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3566T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3566T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3566T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3566T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3566T>C
  variant of: http://identifiers.org/hgnc/2888
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1635-3T>C
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum

1-231910388-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910388
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910388
    reference: chr 1
allele count: 5
allele frequency: 6.641870350690755e-4
allele num: 7528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3572G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3572G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3572G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3572G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1638G>A
  hgvsp: ENST00000535944.1:c.1638G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3572G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3572G>A
  variant of: http://identifiers.org/hgnc/49177
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu546Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

1-231910413-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910413
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910413
    reference: chr 1
allele count: 279
allele frequency: 2.774463007159905e-2
allele num: 10056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3597C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3597C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3597C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3597C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1663C>T
  hgvsp: ENSP00000441193.1:p.Arg555Cys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3597C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3597C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+3597C>T
  variant of: http://identifiers.org/hgnc/2888
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg555Cys
num of homozygotes: 7
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

1-231910414-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910414
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910414
    reference: chr 1
allele count: 2
allele frequency: 1.968891514077574e-4
allele num: 10158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3598G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1664G>A
  hgvsp: ENSP00000441193.1:p.Arg555His
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3598G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3598G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3598G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3598G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3598G>A
  variant of: http://identifiers.org/hgnc/49177
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg555His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ

1-231910414-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910414
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910414
    reference: chr 1
allele count: 1
allele frequency: 9.844457570387872e-5
allele num: 10158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1664G>T
  hgvsp: ENSP00000441193.1:p.Arg555Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3598G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3598G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3598G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3598G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3598G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3598G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3598G>T
  variant of: http://identifiers.org/hgnc/2888
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg555Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

1-231910435-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910435
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910435
    reference: chr 1
allele count: 1
allele frequency: 9.382623381497467e-5
allele num: 10658
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1685C>T
  hgvsp: ENSP00000441193.1:p.Pro562Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3619C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3619C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3619C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3619C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3619C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3619C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3619C>T
  variant of: http://identifiers.org/hgnc/2888
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro562Leu
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

1-231910436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910436
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910436
    reference: chr 1
allele count: 2
allele frequency: 1.874765654293213e-4
allele num: 10668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3620C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3620C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3620C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1686C>T
  hgvsp: ENST00000535944.1:c.1686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3620C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3620C>T
  variant of: http://identifiers.org/hgnc/49177
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro562Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

1-231910473-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910473
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910473
    reference: chr 1
allele count: 1
allele frequency: 9.317927692881103e-5
allele num: 10732
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1723A>G
  hgvsp: ENSP00000441193.1:p.Ile575Val
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3657A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3657A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3657A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3657A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3657A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3657A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3657A>G
  variant of: http://identifiers.org/hgnc/2888
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile575Val
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-231910495-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910495
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910495
    reference: chr 1
allele count: 1
allele frequency: 9.340556697179151e-5
allele num: 10706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1745G>A
  hgvsp: ENSP00000441193.1:p.Gly582Glu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3679G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3679G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3679G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3679G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+3679G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3679G>A
  variant of: http://identifiers.org/hgnc/49177
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly582Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

1-231910496-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910496
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910496
    reference: chr 1
allele count: 1
allele frequency: 9.352787130564908e-5
allele num: 10692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1746G>A
  hgvsp: ENST00000535944.1:c.1746G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3680G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3680G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3680G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3680G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3680G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3680G>A
  variant of: http://identifiers.org/hgnc/2888
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly582Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-231910515-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910515
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910515
    reference: chr 1
allele count: 2
allele frequency: 1.887861053426468e-4
allele num: 10594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-371+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1765G>C
  hgvsp: ENSP00000441193.1:p.Glu589Gln
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3699G>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3699G>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3699G>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3699G>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3699G>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3699G>C
  variant of: http://identifiers.org/hgnc/49177
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu589Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

1-231910603-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231910603
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231910603
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 6016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1764+3787G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1634+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1764+3787G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1634+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1634+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1813+40G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1693+3787G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*493+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1634+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1634+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1495+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*334+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*493+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1634+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1780+3787G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.584+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*493+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1634+3787G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1495+3787G>T
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

1-231930969-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231930969
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231930969
    reference: chr 1
allele count: 35
allele frequency: 2.900616588211894e-4
allele num: 120664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1635-19C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1781-19C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1496-19C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1635-19C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24153C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1765-19C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4885C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-370-19C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1765-19C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1814-19C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23106C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*494-19C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1694-19C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1635-19C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1635-19C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*335-19C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1496-19C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*494-19C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1635-19C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23106C>T
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum

1-231930971-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231930971
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231930971
    reference: chr 1
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1496-17C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*335-17C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23104C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1765-17C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-370-17C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1635-17C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1694-17C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24155C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1496-17C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1635-17C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1635-17C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1635-17C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1765-17C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*494-17C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4883C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1635-17C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1781-17C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1635-17C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1814-17C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*494-17C>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
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: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

1-231930987-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231930987
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231930986
    reference: chr 1
allele count: 1
allele frequency: 8.276501357346223e-6
allele num: 120824
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.1815delC
  hgvsp: ENSP00000441193.1:p.Ser606ProfsTer12
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23086delC
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1636delC
  hgvsp: ENSP00000355596.4:p.Leu546SerfsTer5
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23086delC
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1695delC
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1636delC
  hgvsp: ENSP00000443996.1:p.Leu546SerfsTer5
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1636delC
  hgvsp: ENSP00000355593.3:p.Leu546SerfsTer5
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*336delC
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*495delC
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4865delC
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1782delC
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1636delC
  hgvsp: ENSP00000403888.2:p.Leu546SerfsTer5
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-369delC
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1497delC
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*495delC
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1636delC
  hgvsp: ENSP00000473425.1:p.Leu546SerfsTer5
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1766delC
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1636delC
  hgvsp: ENSP00000440953.1:p.Leu546SerfsTer5
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu546SerfsTer5
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: GC
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

1-231931002-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931002
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931003
    reference: chr 1
allele count: 1
allele frequency: 8.274857672448034e-6
allele num: 120848
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4848dupA
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1653dupA
  hgvsp: ENSP00000473425.1:p.Ser552IlefsTer7
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1653dupA
  hgvsp: ENSP00000440953.1:p.Ser552IlefsTer7
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1653dupA
  hgvsp: ENSP00000355596.4:p.Ser552IlefsTer7
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23069dupA
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1783dupA
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*512dupA
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1514dupA
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1653dupA
  hgvsp: ENSP00000403888.2:p.Ser552IlefsTer7
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1514dupA
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1783dupA
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*2dupA
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24190dupA
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1653dupA
  hgvsp: ENSP00000355593.3:p.Ser552IlefsTer7
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1653dupA
  hgvsp: ENSP00000443996.1:p.Ser552IlefsTer7
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-352dupA
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*512dupA
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23069dupA
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*353dupA
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser552IlefsTer7
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

1-231931013-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931013
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931013
    reference: chr 1
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*519A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1660A>T
  hgvsp: ENSP00000355596.4:p.Asn554Tyr
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4841A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1660A>T
  hgvsp: ENSP00000355593.3:p.Asn554Tyr
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23062A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1719A>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*519A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1521A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1660A>T
  hgvsp: ENSP00000473425.1:p.Asn554Tyr
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1660A>T
  hgvsp: ENSP00000443996.1:p.Asn554Tyr
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1790A>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-345A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1790A>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*9A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1660A>T
  hgvsp: ENSP00000403888.2:p.Asn554Tyr
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1660A>T
  hgvsp: ENSP00000440953.1:p.Asn554Tyr
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*360A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1806A>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24197A>T
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn554Tyr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

1-231931014-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931014
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931014
    reference: chr 1
allele count: 2
allele frequency: 1.656177542232527e-5
allele num: 120760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1661A>G
  hgvsp: ENSP00000473425.1:p.Asn554Ser
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*520A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24198A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*10A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23061A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1522A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1661A>G
  hgvsp: ENSP00000355593.3:p.Asn554Ser
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23061A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1661A>G
  hgvsp: ENSP00000443996.1:p.Asn554Ser
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4840A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1791A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1661A>G
  hgvsp: ENSP00000440953.1:p.Asn554Ser
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1807A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-344A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1661A>G
  hgvsp: ENSP00000355596.4:p.Asn554Ser
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1522A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*520A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*361A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1720A>G
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn554Ser
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

1-231931015-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931015
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931015
    reference: chr 1
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24199C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1662C>G
  hgvsp: ENSP00000440953.1:p.Asn554Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1808C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1662C>G
  hgvsp: ENSP00000473425.1:p.Asn554Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1721C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1792C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-343C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1662C>G
  hgvsp: ENSP00000355593.3:p.Asn554Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1792C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1662C>G
  hgvsp: ENSP00000355596.4:p.Asn554Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4839C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23060C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1662C>G
  hgvsp: ENSP00000443996.1:p.Asn554Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*521C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1523C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*11C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1662C>G
  hgvsp: ENSP00000403888.2:p.Asn554Lys
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1523C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*521C>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn554Lys
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

1-231931022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931022
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931022
    reference: chr 1
allele count: 2
allele frequency: 1.657907389293234e-5
allele num: 120634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*528C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-336C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1669C>T
  hgvsp: ENSP00000355593.3:p.Leu557Phe
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1815C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1669C>T
  hgvsp: ENSP00000440953.1:p.Leu557Phe
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23053C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24206C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1669C>T
  hgvsp: ENSP00000403888.2:p.Leu557Phe
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1669C>T
  hgvsp: ENSP00000473425.1:p.Leu557Phe
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1728C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1530C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1799C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1669C>T
  hgvsp: ENSP00000355596.4:p.Leu557Phe
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1669C>T
  hgvsp: ENSP00000443996.1:p.Leu557Phe
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4832C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*528C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1799C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1530C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23053C>T
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu557Phe
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

1-231931031-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931031
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931031
    reference: chr 1
allele count: 1
allele frequency: 8.312275568559649e-6
allele num: 120304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*27A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1678A>G
  hgvsp: ENSP00000473425.1:p.Ile560Val
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1539A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1678A>G
  hgvsp: ENSP00000440953.1:p.Ile560Val
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24215A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-327A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23044A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*378A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1678A>G
  hgvsp: ENSP00000443996.1:p.Ile560Val
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1737A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1678A>G
  hgvsp: ENSP00000355593.3:p.Ile560Val
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23044A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1678A>G
  hgvsp: ENSP00000355596.4:p.Ile560Val
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1824A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1678A>G
  hgvsp: ENSP00000403888.2:p.Ile560Val
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1808A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*537A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4823A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1539A>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile560Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD

1-231931034-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931034
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931034
    reference: chr 1
allele count: 12
allele frequency: 9.982198412830453e-5
allele num: 120214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1740A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-324A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*30A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23041A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*540A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*381A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1827A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1681A>G
  hgvsp: ENSP00000440953.1:p.Thr561Ala
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1681A>G
  hgvsp: ENSP00000355596.4:p.Thr561Ala
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1681A>G
  hgvsp: ENSP00000443996.1:p.Thr561Ala
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1542A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1542A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1811A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1681A>G
  hgvsp: ENSP00000403888.2:p.Thr561Ala
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1681A>G
  hgvsp: ENSP00000473425.1:p.Thr561Ala
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1681A>G
  hgvsp: ENSP00000355593.3:p.Thr561Ala
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*540A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1811A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4820A>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr561Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

1-231931039-T-TGGGCCGGGCGCGGTGGCTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931039
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931058
    reference: chr 1
allele count: 1
allele frequency: 8.342092530490349e-6
allele num: 119874
alternate allele: TGGGCCGGGCGCGGTGGCTC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsp: ENSP00000440953.1:p.Lys563GlyfsTer73
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsp: ENSP00000355596.4:p.Lys563GlyfsTer12
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsp: ENSP00000355593.3:p.Lys563GlyfsTer12
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsp: ENSP00000443996.1:p.Lys563GlyfsTer12
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsp: ENSP00000403888.2:p.Lys563GlyfsTer12
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsp: ENSP00000473425.1:p.Lys563GlyfsTer12
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys563GlyfsTer12
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: T
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

1-231931040-A-ACGCCTGTAATCCCAGCACTTTGGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931040
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931064
    reference: chr 1
allele count: 1
allele frequency: 8.341953351796856e-6
allele num: 119876
alternate allele: ACGCCTGTAATCCCAGCACTTTGGG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: protein_altering_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: protein altering
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

1-231931048-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931048
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931048
    reference: chr 1
allele count: 14032
allele frequency: 1.180032292787944e-1
allele num: 118912
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24232T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-316+6T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+6T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1550+6T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1689+6T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*548+6T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+6T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1689+6T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*548+6T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*38+6T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1689+6T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1835+6T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*389+6T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1748+6T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1819+6T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4806T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23027T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1689+6T>C
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1689+6T>C
num of homozygotes: 904
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-231931055-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931055
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931055
    reference: chr 1
allele count: 1
allele frequency: 8.504269143109841e-6
allele num: 117588
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*548+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*548+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1689+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24239A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4799A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1550+13A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23020A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1819+13A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1689+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1748+13A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-316+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1689+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*389+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*38+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1689+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1835+13A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1550+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1689+13A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23020A>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

1-231931056-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931056
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931056
    reference: chr 1
allele count: 3
allele frequency: 2.55676007363469e-5
allele num: 117336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23019T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1689+14T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1819+14T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1748+14T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*389+14T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1689+14T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1550+14T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4798T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+14T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*548+14T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-316+14T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23019T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*548+14T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+14T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24240T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*38+14T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1689+14T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1835+14T>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1689+14T>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1689+14T>C
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

1-231931060-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931060
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931060
    reference: chr 1
allele count: 9
allele frequency: 7.699810071351573e-5
allele num: 116886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*548+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1748+18C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-316+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1819+18C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1550+18C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4794C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1550+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24244C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*38+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1689+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23015C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*548+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1835+18C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1689+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1689+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*389+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1689+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1689+18C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+18C>T
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-231931071-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931071
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931071
    reference: chr 1
allele count: 1
allele frequency: 8.648274669203493e-6
allele num: 115630
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1689+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-23004A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-316+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*389+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-23004A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1689+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24255A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1550+29A>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*548+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1689+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1819+29A>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1748+29A>C
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1689+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*38+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4783A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*548+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1689+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1550+29A>C
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1835+29A>C
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

1-231931077-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931077
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931077
    reference: chr 1
allele count: 1
allele frequency: 8.714293183679872e-6
allele num: 114754
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1689+35C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*548+35C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24261C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+35C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1819+35C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1748+35C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-316+35C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+35C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4777C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-22998C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*38+35C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1550+35C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1689+35C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*548+35C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*389+35C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1835+35C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1689+35C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1550+35C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-22998C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1689+35C>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

1-231931091-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231931091
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231931091
    reference: chr 1
allele count: 7
allele frequency: 6.310399538439348e-5
allele num: 110928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-4763G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-316+49G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*548+49G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1550+49G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1819+49G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1550+49G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1835+49G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-22984G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*38+49G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+24275G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-22984G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1689+49G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1748+49G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*389+49G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1689+49G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+49G>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1689+49G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1689+49G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+49G>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*548+49G>A
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-231935822-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935822
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935822
    reference: chr 1
allele count: 1
allele frequency: 8.449942540390725e-6
allele num: 118344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1551-32A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*390-32A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*39-32A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*549-32A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-315-32A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1690-32A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690-32A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18253A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1690-32A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1690-32A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4780A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-32A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820-32A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749-32A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-18253A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29006A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690-32A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+4780A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836-32A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549-32A>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

1-231935825-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935825
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935825
    reference: chr 1
allele count: 16
allele frequency: 1.349937565387601e-4
allele num: 118524
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-18250A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1690-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*39-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29009A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-315-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*390-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4783A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820-29A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749-29A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*549-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1690-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1690-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836-29A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1551-29A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1551-29A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18250A>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-231935828-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935828
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935828
    reference: chr 1
allele count: 1
allele frequency: 8.420627168311495e-6
allele num: 118756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18247A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29012A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1551-26A>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1690-26A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*390-26A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-26A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820-26A>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1551-26A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1690-26A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+4786A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749-26A>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-18247A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549-26A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-315-26A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*549-26A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690-26A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690-26A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4786A>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*39-26A>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836-26A>T
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-231935837-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935837
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935837
    reference: chr 1
allele count: 1
allele frequency: 8.381527114240214e-6
allele num: 119310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+4795C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749-17C>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1690-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18238C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836-17C>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1551-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29021C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-315-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*549-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*390-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-18238C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1690-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820-17C>A
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1690-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*39-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690-17C>A
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4795C>A
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

1-231935837-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935837
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935837
    reference: chr 1
allele count: 3
allele frequency: 2.514458134272064e-5
allele num: 119310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*549-17C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29021C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1551-17C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*390-17C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1690-17C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-315-17C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690-17C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-17C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4795C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549-17C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-18238C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836-17C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749-17C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+4795C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18238C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820-17C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690-17C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*39-17C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1690-17C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1551-17C>T
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

1-231935838-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935838
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935838
    reference: chr 1
allele count: 1
allele frequency: 8.378296859814337e-6
allele num: 119356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749-16A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18237A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1551-16A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29022A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1690-16A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1551-16A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-16A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549-16A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820-16A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*390-16A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-315-16A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1690-16A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690-16A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4796A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690-16A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*549-16A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-18237A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836-16A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+4796A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*39-16A>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

1-231935844-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935844
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935844
    reference: chr 1
allele count: 23
allele frequency: 1.923462902254633e-4
allele num: 119576
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549-10C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690-10C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+4802C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820-10C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1551-10C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1551-10C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4802C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*390-10C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29028C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*549-10C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-10C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-315-10C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836-10C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18231C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690-10C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1690-10C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*39-10C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1690-10C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749-10C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1690-10C>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

1-231935846-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935846
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935846
    reference: chr 1
allele count: 1
allele frequency: 8.360085607276618e-6
allele num: 119616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1690-8C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690-8C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690-8C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+4804C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*549-8C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1551-8C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549-8C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*39-8C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749-8C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820-8C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1690-8C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*390-8C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836-8C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29030C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-18229C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1551-8C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-315-8C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4804C>T
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1690-8C>T
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-231935849-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935849
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935849
    reference: chr 1
allele count: 4
allele frequency: 3.341296757271497e-5
allele num: 119714
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*549-5C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749-5C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549-5C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18226C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*39-5C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690-5C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836-5C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820-5C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-18226C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-315-5C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29033C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-5C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*390-5C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690-5C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1690-5C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1551-5C>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1551-5C>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1690-5C>G
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1690-5C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

1-231935849-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935849
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935849
    reference: chr 1
allele count: 3
allele frequency: 2.505972567953623e-5
allele num: 119714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29033C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*390-5C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690-5C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836-5C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18226C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820-5C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+4807C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1690-5C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-5C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*39-5C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690-5C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549-5C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1551-5C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1690-5C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749-5C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1690-5C>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4807C>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*549-5C>T
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1690-5C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

1-231935850-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935850
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935849
    reference: chr 1
allele count: 1
allele frequency: 8.351846593281774e-6
allele num: 119734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*390-3delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-315-3delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29035delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635-3delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690-3delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1690-3delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690-3delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*39-3delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18224delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749-3delT
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1551-3delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4809delT
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-18224delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1690-3delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836-3delT
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1690-3delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549-3delT
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820-3delT
  variant of: http://identifiers.org/hgnc/49177
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1690-3delT
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: CT
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

1-231935854-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935854
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935854
    reference: chr 1
allele count: 1
allele frequency: 8.345712807330875e-6
allele num: 119822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1820G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18221G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+4812G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-315G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1749G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-18221G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1690G>T
  hgvsp: ENSP00000443996.1:p.Val564Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1635G>T
  hgvsp: ENSP00000295051.7:p.Arg545Ser
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1690G>T
  hgvsp: ENSP00000473425.1:p.Val564Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*549G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1551G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1551G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1690G>T
  hgvsp: ENSP00000403888.2:p.Val564Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29038G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1690G>T
  hgvsp: ENSP00000355596.4:p.Val564Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1690G>T
  hgvsp: ENSP00000355593.3:p.Val564Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1836G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*549G>T
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val564Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-231935858-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935858
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935858
    reference: chr 1
allele count: 21
allele frequency: 1.752248719189627e-4
allele num: 119846
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+4816G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1694G>T
  hgvsp: ENSP00000473425.1:p.Cys565Phe
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1753G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-311G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1694G>T
  hgvsp: ENSP00000355596.4:p.Cys565Phe
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4816G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1639G>T
  hgvsp: ENSP00000295051.7:p.Val547Leu
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1555G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*553G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1694G>T
  hgvsp: ENSP00000355593.3:p.Cys565Phe
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1694G>T
  hgvsp: ENSP00000443996.1:p.Cys565Phe
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18217G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1555G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*43G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473367
  ensembl transcript: ENST00000602962
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602962.1:c.*1824G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1840G>T
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1694G>T
  hgvsp: ENSP00000403888.2:p.Cys565Phe
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473386
  ensembl transcript: ENST00000602873
  gene symbol: DISC1
  hgvsc: ENST00000602873.1:c.585-18217G>T
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*553G>T
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys565Phe
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

1-231935860-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 231935860
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 231935860
    reference: chr 1
allele count: 2
allele frequency: 1.668613382279326e-5
allele num: 119860
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473476
  ensembl transcript: ENST00000602885
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602885.1:c.*1755A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473417
  ensembl transcript: ENST00000602700
  gene symbol: DISC1
  hgvsc: ENST00000602700.1:c.*494-18215A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440953
  ensembl transcript: ENST00000539444
  gene symbol: DISC1
  hgvsc: ENST00000539444.1:c.1689+4818A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355597
  ensembl transcript: ENST00000366637
  gene symbol: DISC1
  hgvsc: ENST00000366637.3:c.-309A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355592
  ensembl transcript: ENST00000366632
  gene symbol: DISC1
  hgvsc: ENST00000366632.2:c.*396A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355593
  ensembl transcript: ENST00000366633
  gene symbol: DISC1
  hgvsc: ENST00000366633.3:c.1696A>G
  hgvsp: ENSP00000355593.3:p.Met566Val
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000403888
  ensembl transcript: ENST00000439617
  gene symbol: DISC1
  hgvsc: ENST00000439617.2:c.1696A>G
  hgvsp: ENSP00000403888.2:p.Met566Val
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000415147
  ensembl transcript: ENST00000422590
  gene symbol: DISC1
  hgvsc: ENST00000422590.2:c.*1557A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000441193
  ensembl transcript: ENST00000535944
  gene symbol: DISC1
  hgvsc: ENST00000535944.1:c.*45A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000443996
  ensembl transcript: ENST00000535983
  gene symbol: DISC1
  hgvsc: ENST00000535983.1:c.1696A>G
  hgvsp: ENSP00000443996.1:p.Met566Val
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473532
  ensembl transcript: ENST00000602956
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602956.1:c.*1557A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473456
  ensembl transcript: ENST00000602567
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602567.1:c.*1819+4818A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473425
  ensembl transcript: ENST00000602281
  gene symbol: DISC1
  hgvsc: ENST00000602281.1:c.1696A>G
  hgvsp: ENSP00000473425.1:p.Met566Val
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000270106
  ensembl protein: ENSP00000473307
  ensembl transcript: ENST00000602634
  gene symbol: TSNAX-DISC1
  hgvsc: ENST00000602634.1:c.*1842A>G
  variant of: http://identifiers.org/hgnc/49177
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000295051
  ensembl transcript: ENST00000295051
  gene symbol: DISC1
  hgvsc: ENST00000295051.7:c.1641A>G
  hgvsp: ENST00000295051.7:c.1641A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473261
  ensembl transcript: ENST00000602713
  gene symbol: DISC1
  hgvsc: ENST00000602713.1:c.*555A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000440909
  ensembl transcript: ENST00000537876
  gene symbol: DISC1
  hgvsc: ENST00000537876.1:c.1634+29044A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000473586
  ensembl transcript: ENST00000602822
  gene symbol: DISC1
  hgvsc: ENST00000602822.1:c.*555A>G
  variant of: http://identifiers.org/hgnc/2888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162946
  ensembl protein: ENSP00000355596
  ensembl transcript: ENST00000366636
  gene symbol: DISC1
  hgvsc: ENST00000366636.4:c.1696A>G
  hgvsp: ENSP00000355596.4:p.Met566Val
  variant of: http://identifiers.org/hgnc/2888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
hgvs: p.Met566Val
num of homozygotes: 0
reference allele: A

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355593
ensembl transcript: ENST00000366633
gene symbol: DISC1
hgvsc: ENST00000366633.3:c.1616C>T
hgvsp: ENSP00000355593.3:p.Pro539Leu
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473586
ensembl transcript: ENST00000602822
gene symbol: DISC1
hgvsc: ENST00000602822.1:c.*475C>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5295
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6880
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23398
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 17093
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3343
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 448
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1291
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1948
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10688
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35629
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1933
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1724
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.753910552985239e-5
allele num: 36312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2816
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.192e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

DP
type: SiteQuality
SIO_000300: 8.68661e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.134e0

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

Annotation
canonical: true
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473532
ensembl transcript: ENST00000602956
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602956.1:c.*1477C>G
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000440909
ensembl transcript: ENST00000537876
gene symbol: DISC1
hgvsc: ENST00000537876.1:c.1616C>G
hgvsp: ENSP00000440909.1:p.Pro539Arg
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1948
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17093
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23398
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5295
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3343
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6880
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 448
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1291
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1724
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35629
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1933
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10688
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 249
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.753910552985239e-5
allele num: 36312
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11204
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.68661e5

QD
type: SiteQuality
SIO_000300: 1.192e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.134e0

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473261
ensembl transcript: ENST00000602713
gene symbol: DISC1
hgvsc: ENST00000602713.1:c.*478C>A
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000441193
ensembl transcript: ENST00000535944
gene symbol: DISC1
hgvsc: ENST00000535944.1:c.1619C>A
hgvsp: ENSP00000441193.1:p.Pro540Gln
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 448
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1235
bin: 3.25e1
variant carriers: 3

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6654
bin: 2.25e1
variant carriers: 3

GenotypeDepth
all individuals: 1798
bin: 1.75e1
variant carriers: 13

GenotypeDepth
all individuals: 185
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3586
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 23742
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17071
bin: 1.25e1
variant carriers: 8

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5164
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36175
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1835
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10694
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 240
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1557
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1202
bin: 9.75e1
variant carriers: 28

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 1.112759643916914e-3
allele num: 2696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 7.050197405527354e-4
allele num: 35460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.022653721682848e-4
allele num: 4944
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11048
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.58564e5

QD
type: SiteQuality
SIO_000300: 1.125e1

FS
type: SiteQuality
SIO_000300: 1.307e0

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.55e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473456
ensembl transcript: ENST00000602567
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602567.1:c.*1749C>G
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473476
ensembl transcript: ENST00000602885
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602885.1:c.*1678C>G
variant of: http://identifiers.org/hgnc/49177

GenotypeDepth
all individuals: 23742
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5164
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17071
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 448
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6654
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1798
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1235
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3586
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 185
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36175
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 240
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1557
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1835
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10694
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4944
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2696
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.820078962210942e-5
allele num: 35460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4536
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

DP
type: SiteQuality
SIO_000300: 8.58564e5

VQSLOD
type: SiteQuality
SIO_000300: 3.4e0

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.307e0

QD
type: SiteQuality
SIO_000300: 1.125e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.55e-2

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355596
ensembl transcript: ENST00000366636
gene symbol: DISC1
hgvsc: ENST00000366636.4:c.1620G>A
hgvsp: ENST00000366636.4:c.1620G>A(p.%3D)
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473261
ensembl transcript: ENST00000602713
gene symbol: DISC1
hgvsc: ENST00000602713.1:c.*479G>A
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1631
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6414
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1178
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5040
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24042
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3869
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 448
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17087
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 166
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36532
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10414
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1795
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 179
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4832
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.867136877114513e-5
allele num: 34878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10912
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 1.011e1

FS
type: SiteQuality
SIO_000300: 4.569e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.17e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

DP
type: SiteQuality
SIO_000300: 8.47787e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.27e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473425
ensembl transcript: ENST00000602281
gene symbol: DISC1
hgvsc: ENST00000602281.1:c.1631G>A
hgvsp: ENSP00000473425.1:p.Arg544Lys
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: true
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473532
ensembl transcript: ENST00000602956
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602956.1:c.*1492G>A
variant of: http://identifiers.org/hgnc/49177

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4474
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1372
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 24705
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 852
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7434
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16500
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3878
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 448
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7418
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1649
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1419
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35535
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1708
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7894
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 275
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.310600542938489e-5
allele num: 30206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3800
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2144
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.303e1

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.74e-2

DP
type: SiteQuality
SIO_000300: 7.64504e5

VQSLOD
type: SiteQuality
SIO_000300: 8.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.288e0

FS
type: SiteQuality
SIO_000300: 3.489e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355597
ensembl transcript: ENST00000366637
gene symbol: DISC1
hgvsc: ENST00000366637.3:c.-371G>A
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000415147
ensembl transcript: ENST00000422590
gene symbol: DISC1
hgvsc: ENST00000422590.2:c.*1495G>A
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: true
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473532
ensembl transcript: ENST00000602956
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602956.1:c.*1495G>A
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473307
ensembl transcript: ENST00000602634
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602634.1:c.*1780G>A
variant of: http://identifiers.org/hgnc/49177

GenotypeDepth
all individuals: 24731
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4074
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15979
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3572
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8707
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1318
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 448
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1782
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1378
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1671
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1174
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9296
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6759
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34635
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28672
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1978
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9574
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.791736460078169e-4
allele num: 3582
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.378e0

DP
type: SiteQuality
SIO_000300: 7.41417e5

QD
type: SiteQuality
SIO_000300: 1.049e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.98e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: -1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.517e0

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355596
ensembl transcript: ENST00000366636
gene symbol: DISC1
hgvsc: ENST00000366636.4:c.1634+7C>G
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473456
ensembl transcript: ENST00000602567
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602567.1:c.*1764+7C>G
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000443996
ensembl transcript: ENST00000535983
gene symbol: DISC1
hgvsc: ENST00000535983.1:c.1634+7C>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 3525
bin: 2.25e1
variant carriers: 4

GenotypeDepth
all individuals: 14429
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 11840
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1198
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2989
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 137
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 449
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 24396
bin: 7.5e0
variant carriers: 6

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 652
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1177
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 480
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12711
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1216
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 32326
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1860
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5678
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3120
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.140250855188141e-4
allele num: 8770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1650
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 2.593774940143655e-3
allele num: 5012
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25276
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.227888960619754e-4
allele num: 3098
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.56e-2

QD
type: SiteQuality
SIO_000300: 1.218e1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 6.93755e5

FS
type: SiteQuality
SIO_000300: 1.296e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.5e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473417
ensembl transcript: ENST00000602700
gene symbol: DISC1
hgvsc: ENST00000602700.1:c.*493+13T>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1222
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2443
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23448
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 12883
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15226
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3003
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 449
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28983
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2107
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1438
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16381
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4646
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1174
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1605
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2718
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1370
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.12e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.44e0

MQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.47271e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.101e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355593
ensembl transcript: ENST00000366633
gene symbol: DISC1
hgvsc: ENST00000366633.3:c.1634+20T>A
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 449
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1926
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11041
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21298
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2419
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19948
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1219
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 133
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 488
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23200
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1132
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21448
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1260
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2503
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3646
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18930
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1952
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2216
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.373042240151875e-4
allele num: 4214
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7214
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.351e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.04e-2

MQ
type: SiteQuality
SIO_000300: 5.887e1

DP
type: SiteQuality
SIO_000300: 5.90357e5

MQRankSum
type: SiteQuality
SIO_000300: 2.04e0

QD
type: SiteQuality
SIO_000300: 1.458e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355596
ensembl transcript: ENST00000366636
gene symbol: DISC1
hgvsc: ENST00000366636.4:c.1634+29G>A
variant of: http://identifiers.org/hgnc/2888

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

GenotypeDepth
all individuals: 1142
bin: 1.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 403
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24672
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2091
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1457
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19707
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 7847
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 449
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16784
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3454
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2807
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25743
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3156
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1141
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 162
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3680
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.117437722419929e-5
allele num: 14050
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

MQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.103e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.85e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.28844e5

MQ
type: SiteQuality
SIO_000300: 5.863e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.419999999999999e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473386
ensembl transcript: ENST00000602873
gene symbol: DISC1
hgvsc: ENST00000602873.1:c.584+31C>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 100
bin: 4.25e1
variant carriers: 41

GenotypeDepth
all individuals: 74
bin: 6.75e1
variant carriers: 10

GenotypeDepth
all individuals: 24893
bin: 2.5e0
variant carriers: 398

GenotypeDepth
all individuals: 1315
bin: 2.75e1
variant carriers: 98

GenotypeDepth
all individuals: 80
bin: 4.75e1
variant carriers: 38

GenotypeDepth
all individuals: 1920
bin: 2.25e1
variant carriers: 184

GenotypeDepth
all individuals: 88
bin: 6.25e1
variant carriers: 19

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 5

GenotypeDepth
all individuals: 513
bin: 9.75e1
variant carriers: 126

GenotypeDepth
all individuals: 377
bin: 3.25e1
variant carriers: 56

GenotypeDepth
all individuals: 19512
bin: 7.5e0
variant carriers: 2748

GenotypeDepth
all individuals: 93
bin: 5.75e1
variant carriers: 11

GenotypeDepth
all individuals: 7300
bin: 1.25e1
variant carriers: 1220

GenotypeDepth
all individuals: 70
bin: 5.25e1
variant carriers: 20

GenotypeDepth
all individuals: 144
bin: 3.75e1
variant carriers: 40

GenotypeDepth
all individuals: 74
bin: 9.25e1
variant carriers: 11

GenotypeDepth
all individuals: 68
bin: 8.25e1
variant carriers: 7

GenotypeDepth
all individuals: 1151
bin: 1.75e1
variant carriers: 344

GenotypeDepth
all individuals: 57
bin: 7.75e1
variant carriers: 4

GenotypeDepth
all individuals: 74
bin: 7.25e1
variant carriers: 12

GenotypeQuality
all individuals: 3120
bin: 2.5e0
variant carriers: 12

GenotypeQuality
all individuals: 14691
bin: 2.25e1
variant carriers: 331

GenotypeQuality
all individuals: 171
bin: 4.25e1
variant carriers: 82

GenotypeQuality
all individuals: 2574
bin: 6.25e1
variant carriers: 74

GenotypeQuality
all individuals: 333
bin: 8.25e1
variant carriers: 260

GenotypeQuality
all individuals: 3266
bin: 9.75e1
variant carriers: 2250

GenotypeQuality
all individuals: 201
bin: 5.75e1
variant carriers: 179

GenotypeQuality
all individuals: 456
bin: 6.75e1
variant carriers: 81

GenotypeQuality
all individuals: 881
bin: 3.25e1
variant carriers: 79

GenotypeQuality
all individuals: 339
bin: 8.75e1
variant carriers: 309

GenotypeQuality
all individuals: 958
bin: 2.75e1
variant carriers: 128

GenotypeQuality
all individuals: 24582
bin: 7.5e0
variant carriers: 145

GenotypeQuality
all individuals: 1967
bin: 1.75e1
variant carriers: 299

GenotypeQuality
all individuals: 2734
bin: 1.25e1
variant carriers: 181

GenotypeQuality
all individuals: 234
bin: 4.75e1
variant carriers: 164

GenotypeQuality
all individuals: 233
bin: 7.25e1
variant carriers: 100

GenotypeQuality
all individuals: 296
bin: 9.25e1
variant carriers: 249

GenotypeQuality
all individuals: 305
bin: 5.25e1
variant carriers: 245

GenotypeQuality
all individuals: 268
bin: 7.75e1
variant carriers: 159

GenotypeQuality
all individuals: 361
bin: 3.75e1
variant carriers: 65

African
type: Population
allele count: 241
allele frequency: 6.69816564758199e-2
allele num: 3598
num of homozygotes: 6

East Asian
type: Population
allele count: 491
allele frequency: 3.095838587641866e-1
allele num: 1586
num of homozygotes: 55

Latino
type: Population
allele count: 388
allele frequency: 3.118971061093248e-1
allele num: 1244
num of homozygotes: 47

European (Non-Finnish)
type: Population
allele count: 612
allele frequency: 4.64128621264978e-2
allele num: 13186
num of homozygotes: 10

European (Finnish)
type: Population
allele count: 33
allele frequency: 5.913978494623656e-2
allele num: 558
num of homozygotes: 0

Other
type: Population
allele count: 28
allele frequency: 1.372549019607843e-1
allele num: 204
num of homozygotes: 2

South Asian
type: Population
allele count: 579
allele frequency: 9.962147281486579e-2
allele num: 5812
num of homozygotes: 23

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.589e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.30364e5

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000441193
ensembl transcript: ENST00000535944
gene symbol: DISC1
hgvsc: ENST00000535944.1:c.1634+32G>A
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 28190
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 136
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 378
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1806
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1315
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17824
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6561
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 444
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 869
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1783
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15761
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 419
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28541
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3066
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.063215610385422e-5
allele num: 12402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.42e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.96634e5

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

QD
type: SiteQuality
SIO_000300: 3.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.377e0

VQSLOD
type: SiteQuality
SIO_000300: -2.815e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: true
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473532
ensembl transcript: ENST00000602956
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602956.1:c.*1495+35C>T
variant of: http://identifiers.org/hgnc/49177

GenotypeDepth
all individuals: 72
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5765
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16819
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 73
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 374
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1212
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29642
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 939
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1628
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 444
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13261
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3535
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29631
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1190
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2342
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2230
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4850
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1076
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.406e1

DP
type: SiteQuality
SIO_000300: 4.76268e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.75e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000415147
ensembl transcript: ENST00000422590
gene symbol: DISC1
hgvsc: ENST00000422590.2:c.*1495+3565G>T
variant of: http://identifiers.org/hgnc/2888

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

GenotypeDepth
all individuals: 2007
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 1683
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2093
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 1097
bin: 1.25e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 19
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 368
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 228
bin: 2.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 2086
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1789
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.1767522855899e-4
allele num: 4594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -6.23e-1

DP
type: SiteQuality
SIO_000300: 8.1572e4

MQ
type: SiteQuality
SIO_000300: 5.911e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.038e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.203e0

QD
type: SiteQuality
SIO_000300: 9.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355596
ensembl transcript: ENST00000366636
gene symbol: DISC1
hgvsc: ENST00000366636.4:c.1634+3566T>C
variant of: http://identifiers.org/hgnc/2888

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

GenotypeDepth
all individuals: 1925
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 353
bin: 1.75e1
variant carriers: 1

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

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

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

GenotypeDepth
all individuals: 1038
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2100
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1826
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 19
bin: 3.25e1
variant carriers: 0

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

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

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

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

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

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

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

GenotypeQuality
all individuals: 1748
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2019
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.09819555182543e-4
allele num: 4766
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.81e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e0

QD
type: SiteQuality
SIO_000300: 1.485e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.3635e4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.466e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.384e0

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473261
ensembl transcript: ENST00000602713
gene symbol: DISC1
hgvsc: ENST00000602713.1:c.*493+3572G>A
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 2269
bin: 2.25e1
variant carriers: 1

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

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

GenotypeDepth
all individuals: 323
bin: 1.75e1
variant carriers: 2

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

GenotypeDepth
all individuals: 334
bin: 2.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 842
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1620
bin: 7.5e0
variant carriers: 1

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

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

GenotypeDepth
all individuals: 2006
bin: 2.5e0
variant carriers: 1

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

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

GenotypeDepth
all individuals: 29
bin: 3.25e1
variant carriers: 1

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

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

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

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

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

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 336
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 280
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1719
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.351351351351351e-2
allele num: 74
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 2.564102564102564e-2
allele num: 156
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5238
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

FS
type: SiteQuality
SIO_000300: 6.534e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.111e1

DP
type: SiteQuality
SIO_000300: 9.0721e4

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.07e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473417
ensembl transcript: ENST00000602700
gene symbol: DISC1
hgvsc: ENST00000602700.1:c.*493+3597C>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 2111
bin: 2.5e0
variant carriers: 8

GenotypeDepth
all individuals: 3
bin: 5.25e1
variant carriers: 3

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

GenotypeDepth
all individuals: 23
bin: 4.25e1
variant carriers: 21

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

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

GenotypeDepth
all individuals: 1024
bin: 2.75e1
variant carriers: 60

GenotypeDepth
all individuals: 454
bin: 7.5e0
variant carriers: 8

GenotypeDepth
all individuals: 3439
bin: 2.25e1
variant carriers: 41

GenotypeDepth
all individuals: 13
bin: 4.75e1
variant carriers: 13

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

GenotypeDepth
all individuals: 214
bin: 1.25e1
variant carriers: 7

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

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

GenotypeDepth
all individuals: 169
bin: 3.25e1
variant carriers: 67

GenotypeDepth
all individuals: 38
bin: 3.75e1
variant carriers: 34

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

GenotypeDepth
all individuals: 117
bin: 1.75e1
variant carriers: 25

GenotypeQuality
all individuals: 268
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 7
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.75e1
variant carriers: 264

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1936
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 177
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3985
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 458
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 2

South Asian
type: Population
allele count: 184
allele frequency: 2.618844292627384e-2
allele num: 7026
num of homozygotes: 6

Other
type: Population
allele count: 5
allele frequency: 4.545454545454546e-2
allele num: 110
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 88
allele frequency: 3.497615262321144e-2
allele num: 2516
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.075268817204301e-2
allele num: 186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.79e-2

DP
type: SiteQuality
SIO_000300: 1.23387e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

QD
type: SiteQuality
SIO_000300: 1.46e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473425
ensembl transcript: ENST00000602281
gene symbol: DISC1
hgvsc: ENST00000602281.1:c.1634+3598G>A
variant of: http://identifiers.org/hgnc/2888

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

GenotypeDepth
all individuals: 1126
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2165
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 89
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 180
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3560
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 127
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 4
bin: 4.25e1
variant carriers: 1

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

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

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

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

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 409
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2011
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4310
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 2

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2536
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.814522938361948e-4
allele num: 7106
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.23276e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.49e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.244e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.95e-1

FS
type: SiteQuality
SIO_000300: 6.558e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

QD
type: SiteQuality
SIO_000300: 1.089e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000443996
ensembl transcript: ENST00000535983
gene symbol: DISC1
hgvsc: ENST00000535983.1:c.1634+3598G>T
variant of: http://identifiers.org/hgnc/2888

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

GenotypeDepth
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 127
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 89
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2165
bin: 2.5e0
variant carriers: 0

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

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

GenotypeDepth
all individuals: 1126
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3560
bin: 2.25e1
variant carriers: 0

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

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

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

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

GenotypeDepth
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 403
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4310
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2011
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 306
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.407261469180974e-4
allele num: 7106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.49e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

QD
type: SiteQuality
SIO_000300: 1.089e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.244e-1

FS
type: SiteQuality
SIO_000300: 6.558e0

DP
type: SiteQuality
SIO_000300: 1.23276e5

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473261
ensembl transcript: ENST00000602713
gene symbol: DISC1
hgvsc: ENST00000602713.1:c.*493+3619C>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 9
bin: 1.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 1

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

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

GenotypeDepth
all individuals: 2168
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3824
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 136
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1333
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4822
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2658
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.338688085676038e-4
allele num: 7470
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

VQSLOD
type: SiteQuality
SIO_000300: -2.101e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.58e-1

DP
type: SiteQuality
SIO_000300: 1.29863e5

FS
type: SiteQuality
SIO_000300: 1.1406e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.047e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.467e1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-2

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473307
ensembl transcript: ENST00000602634
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602634.1:c.*1780+3620C>T
variant of: http://identifiers.org/hgnc/49177

GenotypeDepth
all individuals: 1
bin: 5.75e1
variant carriers: 1

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

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

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

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

GenotypeDepth
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 6.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 146
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2169
bin: 2.5e0
variant carriers: 1

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

GenotypeDepth
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1334
bin: 2.75e1
variant carriers: 0

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

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

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

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

GenotypeDepth
all individuals: 3819
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4826
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7476
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.063829787234043e-2
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2662
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

FS
type: SiteQuality
SIO_000300: 8.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.81e-2

DP
type: SiteQuality
SIO_000300: 1.30053e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.234e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000440953
ensembl transcript: ENST00000539444
gene symbol: DISC1
hgvsc: ENST00000539444.1:c.1634+3657A>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 2059
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 146
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 5.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 3837
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1371
bin: 2.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 350
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4900
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.698224852071006e-4
allele num: 2704
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

FS
type: SiteQuality
SIO_000300: 9.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.73e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.85e-2

DP
type: SiteQuality
SIO_000300: 1.30461e5

MQ
type: SiteQuality
SIO_000300: 5.859e1

QD
type: SiteQuality
SIO_000300: 1.252e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473386
ensembl transcript: ENST00000602873
gene symbol: DISC1
hgvsc: ENST00000602873.1:c.584+3679G>A
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1382
bin: 2.75e1
variant carriers: 0

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

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

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

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

GenotypeDepth
all individuals: 2091
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 137
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3800
bin: 2.25e1
variant carriers: 0

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

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

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

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

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

GenotypeDepth
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 4.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1939
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4874
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 159
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 349
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2690
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.336183858898984e-4
allele num: 7484
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.130000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -5.479000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.64e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.30423e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.004e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473456
ensembl transcript: ENST00000602567
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602567.1:c.*1764+3680G>A
variant of: http://identifiers.org/hgnc/49177

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

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

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

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

GenotypeDepth
all individuals: 2063
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1383
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 139
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 3789
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4859
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1890
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 346
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.337255950788981e-4
allele num: 7478
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.396e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.63e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

FS
type: SiteQuality
SIO_000300: 1.141e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.232e0

MQ
type: SiteQuality
SIO_000300: 5.763e1

DP
type: SiteQuality
SIO_000300: 1.30263e5

QD
type: SiteQuality
SIO_000300: 9.369999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.242e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000443996
ensembl transcript: ENST00000535983
gene symbol: DISC1
hgvsc: ENST00000535983.1:c.1634+3699G>C
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1
bin: 6.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 190
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2026
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

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

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

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

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

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

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

GenotypeDepth
all individuals: 1369
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3676
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 164
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4723
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 2.700513097488523e-4
allele num: 7406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2658
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

DP
type: SiteQuality
SIO_000300: 1.28884e5

QD
type: SiteQuality
SIO_000300: 1.212e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 3.472e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.52e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.0e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355597
ensembl transcript: ENST00000366637
gene symbol: DISC1
hgvsc: ENST00000366637.3:c.-371+3787G>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 617
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2041
bin: 7.5e0
variant carriers: 1

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

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

GenotypeDepth
all individuals: 2382
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2255
bin: 2.5e0
variant carriers: 0

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

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

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

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

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

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

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

GenotypeDepth
all individuals: 14
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 76
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 553
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2514
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 530
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 7.5e0
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1478
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.63e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.538e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.9774e4

QD
type: SiteQuality
SIO_000300: 9.6e0

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355593
ensembl transcript: ENST00000366633
gene symbol: DISC1
hgvsc: ENST00000366633.3:c.1635-19C>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1016
bin: 5.75e1
variant carriers: 3

GenotypeDepth
all individuals: 7167
bin: 3.25e1
variant carriers: 3

GenotypeDepth
all individuals: 712
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2585
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1667
bin: 4.25e1
variant carriers: 7

GenotypeDepth
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 20462
bin: 2.75e1
variant carriers: 5

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17824
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 971
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1360
bin: 4.75e1
variant carriers: 6

GenotypeDepth
all individuals: 259
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 392
bin: 1.75e1
variant carriers: 2

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

GenotypeDepth
all individuals: 742
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1157
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 338
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1739
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 490
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 843
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 6511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2343
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11508
bin: 9.75e1
variant carriers: 35

GenotypeQuality
all individuals: 263
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1930
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.553734061930783e-4
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 4.827565398425007e-4
allele num: 66286
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

FS
type: SiteQuality
SIO_000300: 1.152e0

DP
type: SiteQuality
SIO_000300: 2.091712e6

MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 1.223e1

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473386
ensembl transcript: ENST00000602873
gene symbol: DISC1
hgvsc: ENST00000602873.1:c.585-23104C>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20541
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 7204
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 367
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1738
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1658
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2583
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 668
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1359
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 17805
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1155
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 971
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6506
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 256
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32934
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 174
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11477
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1931
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66310
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.079766536964981e-5
allele num: 16448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.11e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.508e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

DP
type: SiteQuality
SIO_000300: 2.092655e6

MQRankSum
type: SiteQuality
SIO_000300: 9.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e0

Annotation
canonical: true
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473532
ensembl transcript: ENST00000602956
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602956.1:c.*1497delC
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473367
ensembl transcript: ENST00000602962
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602962.1:c.*1766delC
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000440909
ensembl transcript: ENST00000537876
gene symbol: DISC1
hgvsc: ENST00000537876.1:c.1634+24173delC
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1154
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20861
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1658
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18120
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 971
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7207
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1357
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 146
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1738
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2581
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 740
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 120
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1933
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6564
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1133
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11482
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33899
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2345
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 6.732e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

MQ
type: SiteQuality
SIO_000300: 6.045e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.82e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 2.099823e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.45e-1

QD
type: SiteQuality
SIO_000300: 6.51e0

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473307
ensembl transcript: ENST00000602634
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602634.1:c.*1799dupA
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473476
ensembl transcript: ENST00000602885
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602885.1:c.*1712dupA
variant of: http://identifiers.org/hgnc/49177

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

GenotypeDepth
all individuals: 1738
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7196
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1658
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21011
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1154
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 971
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2574
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1357
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 18085
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1014
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11482
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1132
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6588
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2342
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1926
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34050
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505888022166672e-5
allele num: 66406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.101324e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.181e0

VQSLOD
type: SiteQuality
SIO_000300: 7.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e0

FS
type: SiteQuality
SIO_000300: 1.085e0

QD
type: SiteQuality
SIO_000300: 7.75e0

Annotation
canonical: true
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473532
ensembl transcript: ENST00000602956
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602956.1:c.*1521A>T
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473417
ensembl transcript: ENST00000602700
gene symbol: DISC1
hgvsc: ENST00000602700.1:c.*494-23062A>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 972
bin: 6.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1658
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1155
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7189
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 333
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1355
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2575
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17886
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21083
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1738
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6569
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1673
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33907
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11480
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 1916
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66376
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 9.612e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 2.100344e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.428e0

QD
type: SiteQuality
SIO_000300: 2.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.62e-1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473367
ensembl transcript: ENST00000602962
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602962.1:c.*1791A>G
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000403888
ensembl transcript: ENST00000439617
gene symbol: DISC1
hgvsc: ENST00000439617.2:c.1661A>G
hgvsp: ENSP00000403888.2:p.Asn554Ser
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 740
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 363
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1355
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 297
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7193
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1657
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 491
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 21088
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2576
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17829
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1156
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1738
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 259
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2336
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6562
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11481
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33788
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1915
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163061177017911e-4
allele num: 8598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506704836522525e-5
allele num: 66370
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 5.257e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.314e1

MQRankSum
type: SiteQuality
SIO_000300: 7.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

DP
type: SiteQuality
SIO_000300: 2.10004e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473386
ensembl transcript: ENST00000602873
gene symbol: DISC1
hgvsc: ENST00000602873.1:c.585-23060C>G
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355592
ensembl transcript: ENST00000366632
gene symbol: DISC1
hgvsc: ENST00000366632.2:c.*362C>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 298
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1156
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1738
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17840
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7192
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 362
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1658
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 21085
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2574
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1355
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 972
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6558
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11481
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1913
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33883
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506614035616356e-5
allele num: 66374
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.272e0

QD
type: SiteQuality
SIO_000300: 1.44e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

DP
type: SiteQuality
SIO_000300: 2.10004e6

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

VQSLOD
type: SiteQuality
SIO_000300: 5.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000441193
ensembl transcript: ENST00000535944
gene symbol: DISC1
hgvsc: ENST00000535944.1:c.*18C>T
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355592
ensembl transcript: ENST00000366632
gene symbol: DISC1
hgvsc: ENST00000366632.2:c.*369C>T
variant of: http://identifiers.org/hgnc/2888

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

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

GenotypeDepth
all individuals: 972
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1658
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1357
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 17578
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 362
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1738
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1156
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7192
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21072
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2578
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11482
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6522
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 735
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1911
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1665
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33620
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.74246384387524e-4
allele num: 11478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -8.0e-1

FS
type: SiteQuality
SIO_000300: 6.882e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.035e-1

DP
type: SiteQuality
SIO_000300: 2.097549e6

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473586
ensembl transcript: ENST00000602822
gene symbol: DISC1
hgvsc: ENST00000602822.1:c.*537A>G
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473367
ensembl transcript: ENST00000602962
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602962.1:c.*1808A>G
variant of: http://identifiers.org/hgnc/49177

GenotypeDepth
all individuals: 1738
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20952
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2572
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 838
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 453
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 522
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17006
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1355
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7153
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 973
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1157
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1655
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11482
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 732
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 262
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32874
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6450
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512721991952319e-5
allele num: 66106
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.44e0

VQSLOD
type: SiteQuality
SIO_000300: -1.335e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.089718e6

MQ
type: SiteQuality
SIO_000300: 5.575e1

FS
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: -1.374e0

QD
type: SiteQuality
SIO_000300: 8.81e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000440909
ensembl transcript: ENST00000537876
gene symbol: DISC1
hgvsc: ENST00000537876.1:c.1634+24218A>G
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473386
ensembl transcript: ENST00000602873
gene symbol: DISC1
hgvsc: ENST00000602873.1:c.585-23041A>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1738
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 540
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20902
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1359
bin: 4.75e1
variant carriers: 4

GenotypeDepth
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 965
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1159
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7152
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 16793
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 974
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2573
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1656
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 179
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32622
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2303
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1880
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11486
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6401
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.4058106841612e-3
allele num: 8536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66058
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 2.849e0

DP
type: SiteQuality
SIO_000300: 2.087554e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 1407
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1157
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1655
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 686
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20754
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 973
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7126
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2576
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16219
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1355
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1013
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1738
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6331
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11476
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 731
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 168
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31560
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1866
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518095700752976e-5
allele num: 65872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.943e0

MQ
type: SiteQuality
SIO_000300: 5.816e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.515e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

MQRankSum
type: SiteQuality
SIO_000300: -4.791e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

DP
type: SiteQuality
SIO_000300: 2.078749e6

VQSLOD
type: SiteQuality
SIO_000300: -7.889e-1

QD
type: SiteQuality
SIO_000300: 7.7e-1

Annotation
canonical: false
consequence: protein_altering_variant
consequence: splice_region_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000440953
ensembl transcript: ENST00000539444
gene symbol: DISC1
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1409
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2574
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 491
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20760
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1653
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16224
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1355
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 682
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 727
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 1157
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1738
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7120
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 973
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1869
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31695
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1546
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6336
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 321
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11476
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1637
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 276
bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518003521768171e-5
allele num: 65876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.14e-1

DP
type: SiteQuality
SIO_000300: 2.078663e6

QD
type: SiteQuality
SIO_000300: 6.1e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.791e0

VQSLOD
type: SiteQuality
SIO_000300: -7.467e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 4.943e0

MQ
type: SiteQuality
SIO_000300: 5.465e1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000403888
ensembl transcript: ENST00000439617
gene symbol: DISC1
hgvsc: ENST00000439617.2:c.1689+6T>C
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: true
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473532
ensembl transcript: ENST00000602956
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602956.1:c.*1550+6T>C
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473417
ensembl transcript: ENST00000602700
gene symbol: DISC1
hgvsc: ENST00000602700.1:c.*494-23027T>C
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1287
bin: 5.75e1
variant carriers: 506

GenotypeDepth
all individuals: 638
bin: 7.75e1
variant carriers: 161

GenotypeDepth
all individuals: 12805
bin: 2.25e1
variant carriers: 950

GenotypeDepth
all individuals: 2782
bin: 1.25e1
variant carriers: 108

GenotypeDepth
all individuals: 41
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 6855
bin: 3.25e1
variant carriers: 1823

GenotypeDepth
all individuals: 1100
bin: 7.5e0
variant carriers: 20

GenotypeDepth
all individuals: 778
bin: 7.25e1
variant carriers: 188

GenotypeDepth
all individuals: 1613
bin: 5.25e1
variant carriers: 730

GenotypeDepth
all individuals: 18657
bin: 2.75e1
variant carriers: 1560

GenotypeDepth
all individuals: 510
bin: 8.25e1
variant carriers: 160

GenotypeDepth
all individuals: 383
bin: 8.75e1
variant carriers: 139

GenotypeDepth
all individuals: 3220
bin: 3.75e1
variant carriers: 1899

GenotypeDepth
all individuals: 1147
bin: 6.25e1
variant carriers: 359

GenotypeDepth
all individuals: 1146
bin: 1.75e1
variant carriers: 400

GenotypeDepth
all individuals: 937
bin: 6.75e1
variant carriers: 263

GenotypeDepth
all individuals: 2491
bin: 4.25e1
variant carriers: 1599

GenotypeDepth
all individuals: 2084
bin: 9.75e1
variant carriers: 1098

GenotypeDepth
all individuals: 269
bin: 9.25e1
variant carriers: 111

GenotypeDepth
all individuals: 1960
bin: 4.75e1
variant carriers: 1089

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 13

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 513
bin: 9.25e1
variant carriers: 52

GenotypeQuality
all individuals: 2600
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 26283
bin: 6.25e1
variant carriers: 41

GenotypeQuality
all individuals: 353
bin: 5.75e1
variant carriers: 19

GenotypeQuality
all individuals: 376
bin: 5.25e1
variant carriers: 28

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 6

GenotypeQuality
all individuals: 1146
bin: 7.75e1
variant carriers: 36

GenotypeQuality
all individuals: 787
bin: 3.25e1
variant carriers: 14

GenotypeQuality
all individuals: 635
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 221
bin: 4.75e1
variant carriers: 20

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 344
bin: 8.75e1
variant carriers: 30

GenotypeQuality
all individuals: 1140
bin: 7.25e1
variant carriers: 38

GenotypeQuality
all individuals: 812
bin: 8.25e1
variant carriers: 66

GenotypeQuality
all individuals: 4678
bin: 6.75e1
variant carriers: 33

GenotypeQuality
all individuals: 429
bin: 3.75e1
variant carriers: 9

GenotypeQuality
all individuals: 20020
bin: 9.75e1
variant carriers: 12735

East Asian
type: Population
allele count: 999
allele frequency: 1.186179054856329e-1
allele num: 8422
num of homozygotes: 60

Other
type: Population
allele count: 97
allele frequency: 1.092342342342342e-1
allele num: 888
num of homozygotes: 7

African
type: Population
allele count: 1139
allele frequency: 1.122167487684729e-1
allele num: 10150
num of homozygotes: 67

European (Non-Finnish)
type: Population
allele count: 8978
allele frequency: 1.374295860886603e-1
allele num: 65328
num of homozygotes: 616

European (Finnish)
type: Population
allele count: 852
allele frequency: 1.303549571603427e-1
allele num: 6536
num of homozygotes: 66

South Asian
type: Population
allele count: 1073
allele frequency: 6.588480903843792e-2
allele num: 16286
num of homozygotes: 45

Latino
type: Population
allele count: 894
allele frequency: 7.91010440629977e-2
allele num: 11302
num of homozygotes: 43

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

DP
type: SiteQuality
SIO_000300: 2.167913e6

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.37e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

FS
type: SiteQuality
SIO_000300: 6.36e-1

QD
type: SiteQuality
SIO_000300: 1.578e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473456
ensembl transcript: ENST00000602567
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602567.1:c.*1819+13A>G
variant of: http://identifiers.org/hgnc/49177

GenotypeDepth
all individuals: 5370
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12764
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1785
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1094
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1113
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21796
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1501
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1672
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1089
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 956
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6363
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1201
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 402
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 960
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1218
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 935
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5694
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31792
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1530
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4756
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8935
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55077228459773e-5
allele num: 64484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.71e-1

DP
type: SiteQuality
SIO_000300: 1.898451e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.179e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.49e0

FS
type: SiteQuality
SIO_000300: 1.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.029e0

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000415147
ensembl transcript: ENST00000422590
gene symbol: DISC1
hgvsc: ENST00000422590.2:c.*1550+14T>C
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 402
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1879
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 956
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1201
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6275
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1089
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1115
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21243
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12283
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6069
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1663
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1093
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 960
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1817
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5185
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1808
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8937
bin: 9.75e1
variant carriers: 3

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

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

GenotypeQuality
all individuals: 956
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30371
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5565
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.664034078542334e-5
allele num: 64322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

DP
type: SiteQuality
SIO_000300: 1.88423e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

MQRankSum
type: SiteQuality
SIO_000300: -8.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

QD
type: SiteQuality
SIO_000300: 1.611e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473417
ensembl transcript: ENST00000602700
gene symbol: DISC1
hgvsc: ENST00000602700.1:c.*494-23015C>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 7202
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5992
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1650
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 151
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2041
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1202
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2308
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 954
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1111
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20390
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 402
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 11610
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1094
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 181
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1090
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5117
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5865
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8938
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29299
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11114
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.405283867341203e-4
allele num: 64044
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.595e0

VQSLOD
type: SiteQuality
SIO_000300: 4.07e0

QD
type: SiteQuality
SIO_000300: 1.137e1

DP
type: SiteQuality
SIO_000300: 1.860084e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473456
ensembl transcript: ENST00000602567
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602567.1:c.*1819+29A>C
variant of: http://identifiers.org/hgnc/49177

GenotypeDepth
all individuals: 8750
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1099
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4741
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1089
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2421
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11608
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1092
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1563
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 960
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 954
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6618
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15281
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 402
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 687
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1200
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3317
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4744
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21009
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8924
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 830
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7769
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3011
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 7.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.22975330176925e-5
allele num: 16052
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63300
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

QD
type: SiteQuality
SIO_000300: 1.496e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

VQSLOD
type: SiteQuality
SIO_000300: 9.19e-1

DP
type: SiteQuality
SIO_000300: 1.74456e6

MQRankSum
type: SiteQuality
SIO_000300: 7.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355596
ensembl transcript: ENST00000366636
gene symbol: DISC1
hgvsc: ENST00000366636.4:c.1689+35C>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1092
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4013
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7819
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1087
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 951
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 504
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12451
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9931
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2622
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1200
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 12524
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1504
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 685
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1089
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 814
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8037
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17497
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5884
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8914
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3416
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4621
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3346
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.017087062652563e-4
allele num: 9832
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62798
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

FS
type: SiteQuality
SIO_000300: 3.148e0

DP
type: SiteQuality
SIO_000300: 1.691718e6

QD
type: SiteQuality
SIO_000300: 1.484e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473425
ensembl transcript: ENST00000602281
gene symbol: DISC1
hgvsc: ENST00000602281.1:c.1689+49G>A
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 685
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15175
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1086
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1423
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 814
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 597
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3950
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11824
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1199
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5508
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1086
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 182
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2497
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10367
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 570
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1088
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 951
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3752
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3447
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5575
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6578
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6965
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7092
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5433
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2188
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8916
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3254
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1056
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.615506747816882e-5
allele num: 60464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.916687963199591e-4
allele num: 15652
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.375e1

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

FS
type: SiteQuality
SIO_000300: 5.776e0

DP
type: SiteQuality
SIO_000300: 1.596905e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.87e-1

Annotation
canonical: true
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473532
ensembl transcript: ENST00000602956
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602956.1:c.*1551-32A>G
variant of: http://identifiers.org/hgnc/49177

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21103
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14213
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2050
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1263
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 949
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 772
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 348
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3085
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3003
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7050
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1532
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28725
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6726
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2997
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10511
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 938
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.934432743890324e-5
allele num: 10066
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64818
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11176
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.465e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.459e0

DP
type: SiteQuality
SIO_000300: 2.039819e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.279e0

VQSLOD
type: SiteQuality
SIO_000300: -2.788e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 6.435e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000440953
ensembl transcript: ENST00000539444
gene symbol: DISC1
hgvsc: ENST00000539444.1:c.1689+4783A>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21563
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 703
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1619
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14591
bin: 2.75e1
variant carriers: 4

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 352
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3004
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 561
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 861
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 950
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7111
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3096
bin: 3.75e1
variant carriers: 4

GenotypeDepth
all individuals: 1537
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 853
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3006
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6790
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10524
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 703
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29574
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 4.459507670353193e-4
allele num: 11212
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.217433649866082e-4
allele num: 16428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.38687706105341e-4
allele num: 64894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

QD
type: SiteQuality
SIO_000300: 1.496e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.647e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

DP
type: SiteQuality
SIO_000300: 2.05058e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000443996
ensembl transcript: ENST00000535983
gene symbol: DISC1
hgvsc: ENST00000535983.1:c.1690-26A>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 587
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3102
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 579
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7174
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 369
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3004
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1536
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 949
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22054
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 624
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14836
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1217
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30088
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10511
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 227
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3012
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6824
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2396
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537751806858373e-5
allele num: 65030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11242
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.059702e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.835e0

MQRankSum
type: SiteQuality
SIO_000300: 9.08e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

QD
type: SiteQuality
SIO_000300: 1.631e1

VQSLOD
type: SiteQuality
SIO_000300: 6.900000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.86e-1

Annotation
canonical: true
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473532
ensembl transcript: ENST00000602956
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602956.1:c.*1551-17C>A
variant of: http://identifiers.org/hgnc/49177

GenotypeDepth
all individuals: 15487
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 329
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3119
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 952
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1541
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7313
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 461
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22670
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3005
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 560
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2422
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6933
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3026
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10517
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 175
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31766
bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531159087429184e-5
allele num: 65310
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.735e0

FS
type: SiteQuality
SIO_000300: 3.076e0

DP
type: SiteQuality
SIO_000300: 2.078774e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.13e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

QD
type: SiteQuality
SIO_000300: 1.254e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473425
ensembl transcript: ENST00000602281
gene symbol: DISC1
hgvsc: ENST00000602281.1:c.1690-17C>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 952
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 329
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7313
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 560
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1541
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 461
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15487
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 174
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3119
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22670
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3005
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 315
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3026
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10517
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 31766
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2422
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6933
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.062318174858368e-5
allele num: 65310
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.837044892188053e-5
allele num: 11316
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.078774e6

QD
type: SiteQuality
SIO_000300: 1.254e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.735e0

FS
type: SiteQuality
SIO_000300: 3.076e0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.13e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000443996
ensembl transcript: ENST00000535983
gene symbol: DISC1
hgvsc: ENST00000535983.1:c.1690-16A>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 951
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7303
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15535
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3006
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 394
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 314
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22778
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 126
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3113
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1536
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 856
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6975
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10518
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32022
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3033
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.883e0

FS
type: SiteQuality
SIO_000300: 2.093e0

VQSLOD
type: SiteQuality
SIO_000300: -6.482e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

DP
type: SiteQuality
SIO_000300: 2.079885e6

MQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e0

QD
type: SiteQuality
SIO_000300: 1.693e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473386
ensembl transcript: ENST00000602873
gene symbol: DISC1
hgvsc: ENST00000602873.1:c.585-18231C>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 218
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1544
bin: 4.25e1
variant carriers: 5

GenotypeDepth
all individuals: 218
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 956
bin: 4.75e1
variant carriers: 4

GenotypeDepth
all individuals: 3130
bin: 3.75e1
variant carriers: 4

GenotypeDepth
all individuals: 22900
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 380
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3006
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 522
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 66
bin: 1.75e1
variant carriers: 3

GenotypeDepth
all individuals: 7347
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 624
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15678
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32337
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6992
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 10539
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3028
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

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

Latino
type: Population
allele count: 23
allele frequency: 2.018252018252018e-3
allele num: 11396
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

QD
type: SiteQuality
SIO_000300: 1.575e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 4.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

DP
type: SiteQuality
SIO_000300: 2.085298e6

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000295051
ensembl transcript: ENST00000295051
gene symbol: DISC1
hgvsc: ENST00000295051.7:c.1635-8C>T
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473417
ensembl transcript: ENST00000602700
gene symbol: DISC1
hgvsc: ENST00000602700.1:c.*494-18229C>T
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000403888
ensembl transcript: ENST00000439617
gene symbol: DISC1
hgvsc: ENST00000439617.2:c.1690-8C>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7371
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22895
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3129
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15744
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 950
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1546
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3006
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6983
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3024
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2426
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32431
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10518
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528864970645792e-5
allele num: 65408
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.24e-1

MQ
type: SiteQuality
SIO_000300: 5.914e1

MQRankSum
type: SiteQuality
SIO_000300: -5.55e-1

FS
type: SiteQuality
SIO_000300: 2.257e0

QD
type: SiteQuality
SIO_000300: 1.537e1

DP
type: SiteQuality
SIO_000300: 2.086515e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.241e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000440953
ensembl transcript: ENST00000539444
gene symbol: DISC1
hgvsc: ENST00000539444.1:c.1689+4807C>G
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473456
ensembl transcript: ENST00000602567
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602567.1:c.*1819+4807C>G
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000403888
ensembl transcript: ENST00000439617
gene symbol: DISC1
hgvsc: ENST00000439617.2:c.1690-5C>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 15831
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 951
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1540
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7371
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 22916
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3127
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 625
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3006
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32622
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6998
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3026
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10527
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527883880825057e-5
allele num: 65450
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.621461027612723e-4
allele num: 11444
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.07e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

DP
type: SiteQuality
SIO_000300: 2.088305e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.14e0

VQSLOD
type: SiteQuality
SIO_000300: 6.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473386
ensembl transcript: ENST00000602873
gene symbol: DISC1
hgvsc: ENST00000602873.1:c.585-18226C>T
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000415147
ensembl transcript: ENST00000422590
gene symbol: DISC1
hgvsc: ENST00000422590.2:c.*1551-5C>T
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355597
ensembl transcript: ENST00000366637
gene symbol: DISC1
hgvsc: ENST00000366637.3:c.-315-5C>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 7371
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15831
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 625
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3006
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3127
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22916
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1540
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 951
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32622
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3026
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6998
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10527
bin: 9.75e1
variant carriers: 3

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.958863858961802e-4
allele num: 10210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527883880825057e-5
allele num: 65450
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.07e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: 6.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.231e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.14e0

DP
type: SiteQuality
SIO_000300: 2.088305e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000440953
ensembl transcript: ENST00000539444
gene symbol: DISC1
hgvsc: ENST00000539444.1:c.1689+4809delT
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: true
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473532
ensembl transcript: ENST00000602956
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602956.1:c.*1551-3delT
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473261
ensembl transcript: ENST00000602713
gene symbol: DISC1
hgvsc: ENST00000602713.1:c.*549-3delT
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 7370
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 393
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3007
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 950
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22934
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15847
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3129
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1537
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3028
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2419
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10522
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 7011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32668
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527557130636686e-5
allele num: 65464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.088e1

FS
type: SiteQuality
SIO_000300: 5.298e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

DP
type: SiteQuality
SIO_000300: 2.088479e6

QD
type: SiteQuality
SIO_000300: 1.394e1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000441193
ensembl transcript: ENST00000535944
gene symbol: DISC1
hgvsc: ENST00000535944.1:c.*39G>T
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473456
ensembl transcript: ENST00000602567
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602567.1:c.*1819+4812G>T
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355592
ensembl transcript: ENST00000366632
gene symbol: DISC1
hgvsc: ENST00000366632.2:c.*390G>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3007
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1538
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15899
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 507
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22978
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 950
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3129
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7378
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32764
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3032
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7020
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10520
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2422
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1999
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526764176005374e-5
allele num: 65498
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.54e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
SIO_000300: 2.090138e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

FS
type: SiteQuality
SIO_000300: 2.259e0

QD
type: SiteQuality
SIO_000300: 1.541e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.045e0

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000355592
ensembl transcript: ENST00000366632
gene symbol: DISC1
hgvsc: ENST00000366632.2:c.*394G>T
variant of: http://identifiers.org/hgnc/2888

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000440909
ensembl transcript: ENST00000537876
gene symbol: DISC1
hgvsc: ENST00000537876.1:c.1634+29042G>T
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 1543
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 512
bin: 5.75e1
variant carriers: 5

GenotypeDepth
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22940
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 954
bin: 4.75e1
variant carriers: 4

GenotypeDepth
all individuals: 15943
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 627
bin: 5.25e1
variant carriers: 4

GenotypeDepth
all individuals: 3134
bin: 3.75e1
variant carriers: 5

GenotypeDepth
all individuals: 7384
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3006
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 635
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7019
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2425
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10541
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1998
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32796
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.221224888563229e-4
allele num: 65508
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.131615598885794e-3
allele num: 11488
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.97e-1

DP
type: SiteQuality
SIO_000300: 2.091522e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.925e1

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.916e0

FS
type: SiteQuality
SIO_000300: 4.751e0

QD
type: SiteQuality
SIO_000300: 1.252e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000270106
ensembl protein: ENSP00000473367
ensembl transcript: ENST00000602962
gene symbol: TSNAX-DISC1
hgvsc: ENST00000602962.1:c.*1826A>G
variant of: http://identifiers.org/hgnc/49177

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000162946
ensembl protein: ENSP00000473386
ensembl transcript: ENST00000602873
gene symbol: DISC1
hgvsc: ENST00000602873.1:c.585-18215A>G
variant of: http://identifiers.org/hgnc/2888

GenotypeDepth
all individuals: 478
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22957
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15969
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7382
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 507
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1536
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3132
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 559
bin: 7.75e1
variant carriers: 0