14-102698003-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698003
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698003
    reference: chr 14
allele count: 4
allele frequency: 3.317354741329264e-5
allele num: 120578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+2022C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+869C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+869C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+869C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1060C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1623+41C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.559+41C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1619+41C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+869C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+41C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+41C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+869C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.294-2009C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+41C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+41C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+869C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+869C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.488+41C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+869C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2168+41C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+869C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

14-102698006-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698006
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698006
    reference: chr 14
allele count: 1
allele frequency: 8.290361625574107e-6
allele num: 120622
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+866A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+38A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+866A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+866A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+866A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+2019A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+38A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+866A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1619+38A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1057A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.294-2012A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+38A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+38A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+866A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.115+38A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+866A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2168+38A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.559+38A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1623+38A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+866A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+866A>G
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

14-102698011-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698011
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698011
    reference: chr 14
allele count: 1
allele frequency: 8.286789200656313e-6
allele num: 120674
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+861A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+861A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+861A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+861A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+33A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+861A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+861A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1619+33A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+2014A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+33A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1623+33A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+33A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.891+33A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.115+33A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+861A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1052A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+33A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+861A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+861A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+2014A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2168+33A>C
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

14-102698015-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698015
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698015
    reference: chr 14
allele count: 2
allele frequency: 1.65809981760902e-5
allele num: 120620
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.891+29G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+29G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+857G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+857G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.488+29G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+857G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.559+29G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+857G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+857G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+2010G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+29G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+857G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+857G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2168+29G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+29G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1048G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1619+29G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+857G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+857G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+857G>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+857G>C
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

14-102698022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698022
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698022
    reference: chr 14
allele count: 6
allele frequency: 4.969191015702644e-5
allele num: 120744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1623+22G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+850G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+850G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+850G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+850G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+850G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1619+22G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+850G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+22G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.559+22G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+22G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+850G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+850G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+850G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+2003G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.115+22G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+2003G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1041G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+850G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+850G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+22G>A
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

14-102698023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698023
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698023
    reference: chr 14
allele count: 8
allele frequency: 6.622845505571468e-5
allele num: 120794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+849C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+21C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+21C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1040C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+849C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+849C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+21C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+849C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+849C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+21C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+2002C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.488+21C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+849C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+849C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+2002C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.559+21C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+849C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+849C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2168+21C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.891+21C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+849C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-102698028-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698028
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698028
    reference: chr 14
allele count: 6
allele frequency: 4.964421644878372e-5
allele num: 120860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.891+16G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+16G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1035G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.488+16G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+16G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.115+16G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+844G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1997G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+844G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.559+16G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+844G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1997G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1619+16G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+16G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+16G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+844G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+844G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2168+16G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1623+16G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+844G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+844G>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

14-102698028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698028
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698028
    reference: chr 14
allele count: 3
allele frequency: 2.482210822439186e-5
allele num: 120860
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+844G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+844G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+844G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+844G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1997G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1035G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+844G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.115+16G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2168+16G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+844G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+16G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+844G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+16G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+844G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+16G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.559+16G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+16G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1619+16G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+844G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.891+16G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+844G>A
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-102698029-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698029
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698029
    reference: chr 14
allele count: 2
allele frequency: 1.654341820106871e-5
allele num: 120894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1619+15C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+843C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+15C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1034C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1996C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+15C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+15C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+843C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+843C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.891+15C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+843C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+843C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.115+15C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+15C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+843C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+843C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.488+15C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1623+15C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.559+15C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+843C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+843C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/14-102698034-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698034
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698034
    reference: chr 14
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1991G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1029G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+838G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+838G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+838G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+10G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.488+10G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1623+10G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+838G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1619+10G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+838G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+10G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.891+10G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+838G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+10G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+838G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2168+10G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.115+10G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+10G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+838G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+838G>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

14-102698034-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698034
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698034
    reference: chr 14
allele count: 9158
allele frequency: 7.570346857123962e-2
allele num: 120972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+838G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.488+10G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+838G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+10G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+838G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+838G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1991G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.891+10G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1619+10G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+838G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+838G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1991G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+10G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+10G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+838G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1029G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+838G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.115+10G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1623+10G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+10G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+838G>A
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 424
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-102698035-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698035
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698035
    reference: chr 14
allele count: 3
allele frequency: 2.479871707970308e-5
allele num: 120974
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.891+9C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+9C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+837C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+837C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+9C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+837C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2168+9C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+837C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1619+9C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1990C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.488+9C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+837C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1623+9C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+837C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1028C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+837C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+9C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+837C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.559+9C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+837C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+9C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

14-102698036-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698036
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698035
    reference: chr 14
allele count: 3
allele frequency: 2.47950277704311e-5
allele num: 120992
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+835delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2168+7delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1988delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1968+7delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.514+7delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+835delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+835delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.978+7delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+835delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.559+7delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1988delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.891+7delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.115+7delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.488+7delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+835delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1026delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.981+7delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1623+7delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+835delA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+835delA
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.981+7delA
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: CT
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

14-102698060-TTGGAAATCTGGC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698060
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698048
    reference: chr 14
allele count: 1
allele frequency: 8.265282507356101e-6
allele num: 120988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: stop_gained
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: stop_gained
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: stop_gained
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  consequence: stop_gained
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys318_Lys322delinsTer
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: TTGGAAATCTGGC
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

14-102698062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698062
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698062
    reference: chr 14
allele count: 1
allele frequency: 8.266102367411717e-6
allele num: 120976
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.1001C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.960C>T
  hgvsp: ENST00000522874.1:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2150C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.97C>T
  hgvsp: ENST00000521937.1:c.97C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.963C>T
  hgvsp: ENST00000361847.2:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1601C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1963C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1950C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+810C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1605C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.470C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+810C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+810C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.873C>T
  hgvsp: ENST00000524214.1:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+810C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.541C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+810C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+810C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.496C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+810C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser321Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

14-102698069-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698069
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698069
    reference: chr 14
allele count: 1
allele frequency: 8.268699664290793e-6
allele num: 120938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2143A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.953A>G
  hgvsp: ENSP00000429469.1:p.Gln318Arg
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+803A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+803A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.866A>G
  hgvsp: ENSP00000428942.1:p.Gln289Arg
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.994A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.489A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+803A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.90A>G
  hgvsp: ENSP00000430416.1:p.Gln31Arg
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1956A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1598A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1943A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+803A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+803A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1594A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+803A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.463A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+803A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.534A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.956A>G
  hgvsp: ENSP00000355304.2:p.Gln319Arg
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln319Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-102698071-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698071
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698071
    reference: chr 14
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+801C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.461C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+801C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+801C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1596C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1954C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+801C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+801C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+801C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1592C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+801C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.954C>G
  hgvsp: ENSP00000355304.2:p.Cys318Trp
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.487C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1954C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.864C>G
  hgvsp: ENSP00000428942.1:p.Cys288Trp
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.532C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+801C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2141C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.992C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.88C>G
  hgvsp: ENSP00000430416.1:p.Cys30Trp
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1941C>G
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys318Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

14-102698079-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698079
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698079
    reference: chr 14
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.856A>G
  hgvsp: ENSP00000428942.1:p.Asn286Asp
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+793A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1588A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+793A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.524A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+793A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+793A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.984A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1584A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1946A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.80A>G
  hgvsp: ENSP00000430416.1:p.Asn28Asp
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.946A>G
  hgvsp: ENSP00000355304.2:p.Asn316Asp
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.479A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.943A>G
  hgvsp: ENSP00000429469.1:p.Asn315Asp
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2133A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1933A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+793A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+793A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+793A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1946A>G
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn316Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-102698079-T-TGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698079
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698081
    reference: chr 14
allele count: 447
allele frequency: 3.696353262217812e-3
allele num: 120930
alternate allele: TGA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.523_524insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.79_80insTC
  hgvsp: ENSP00000430416.1:p.Asn28SerfsTer17
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+792_64+793insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.855_856insTC
  hgvsp: ENSP00000428942.1:p.Asn286SerfsTer17
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+792_164+793insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1945_293+1946insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+792_64+793insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+792_64+793insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+792_64+793insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+792_64+793insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.942_943insTC
  hgvsp: ENSP00000429469.1:p.Asn315SerfsTer17
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.983_984insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1932_1933insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+792_504+793insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1583_*1584insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+792_64+793insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.478_479insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+792_64+793insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1587_1588insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.452_453insTC
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.945_946insTC
  hgvsp: ENSP00000355304.2:p.Asn316SerfsTer17
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn316SerfsTer17
num of homozygotes: 12
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

14-102698091-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698091
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698091
    reference: chr 14
allele count: 19
allele frequency: 1.572222957765127e-4
allele num: 120848
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1572G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+781G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1921G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+781G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.931G>A
  hgvsp: ENSP00000429469.1:p.Glu311Lys
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.68G>A
  hgvsp: ENSP00000430416.1:p.Glu24Lys
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1576G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.844G>A
  hgvsp: ENSP00000428942.1:p.Glu282Lys
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+781G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+781G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+781G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+781G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2121G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.671G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.512G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.934G>A
  hgvsp: ENSP00000355304.2:p.Glu312Lys
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.441G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.467G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+781G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1934G>A
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu312Lys
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

14-102698093-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698093
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698093
    reference: chr 14
allele count: 9
allele frequency: 7.450701193767902e-5
allele num: 120794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1574C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.66C>T
  hgvsp: ENSP00000430416.1:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.669C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.932C>T
  hgvsp: ENSP00000355304.2:p.Pro311Leu
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.929C>T
  hgvsp: ENSP00000429469.1:p.Pro310Leu
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2119C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+779C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+779C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1932C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+779C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+779C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1919C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.970C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.465C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1570C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.842C>T
  hgvsp: ENSP00000428942.1:p.Pro281Leu
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+779C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.510C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+779C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+779C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+779C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro311Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP

14-102698094-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698094
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698094
    reference: chr 14
allele count: 4
allele frequency: 3.311532411623479e-5
allele num: 120790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.65C>T
  hgvsp: ENSP00000430416.1:p.Pro23Ser
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1931C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.928C>T
  hgvsp: ENSP00000429469.1:p.Pro310Ser
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.931C>T
  hgvsp: ENSP00000355304.2:p.Pro311Ser
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1931C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1918C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.668C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+778C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+778C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+778C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.464C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2118C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.438C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1569C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+778C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.841C>T
  hgvsp: ENSP00000428942.1:p.Pro281Ser
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.969C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+778C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+778C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+778C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro311Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

14-102698102-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698102
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698102
    reference: chr 14
allele count: 2
allele frequency: 1.656342134031205e-5
allele num: 120748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.456C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.660C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+770C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+770C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1910C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.833C>G
  hgvsp: ENSP00000428942.1:p.Pro278Arg
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.923C>G
  hgvsp: ENSP00000355304.2:p.Pro308Arg
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.430C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2110C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.920C>G
  hgvsp: ENSP00000429469.1:p.Pro307Arg
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.501C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+770C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+770C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.961C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+770C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.57C>G
  hgvsp: ENSP00000430416.1:p.Pro20Arg
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+770C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1561C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1565C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+770C>G
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro308Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-102698103-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698103
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698103
    reference: chr 14
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+769C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+769C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+769C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2109C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.832C>G
  hgvsp: ENSP00000428942.1:p.Pro278Ala
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1560C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.922C>G
  hgvsp: ENSP00000355304.2:p.Pro308Ala
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.919C>G
  hgvsp: ENSP00000429469.1:p.Pro307Ala
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.429C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+769C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1922C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.56C>G
  hgvsp: ENSP00000430416.1:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.455C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1564C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1909C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.500C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.659C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+769C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+769C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+769C>G
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro308Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-102698110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698110
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698110
    reference: chr 14
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+762G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+762G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.422G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1915G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.493G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+762G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+762G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.49G>A
  hgvsp: ENST00000521937.1:c.49G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2102G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.912G>A
  hgvsp: ENST00000522874.1:c.912G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.915G>A
  hgvsp: ENST00000361847.2:c.915G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+762G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+762G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.825G>A
  hgvsp: ENST00000524214.1:c.825G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1902G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+762G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.953G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+762G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+762G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.652G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1915G>A
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro305Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

14-102698111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698111
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698111
    reference: chr 14
allele count: 10
allele frequency: 8.287888080359362e-5
allele num: 120658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.824C>T
  hgvsp: ENSP00000428942.1:p.Pro275Leu
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.952C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.421C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+761C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2101C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.447C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.651C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+761C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1914C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+761C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+761C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+761C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1901C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.914C>T
  hgvsp: ENSP00000355304.2:p.Pro305Leu
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+761C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1914C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.911C>T
  hgvsp: ENSP00000429469.1:p.Pro304Leu
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.492C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+761C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1552C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.48C>T
  hgvsp: ENSP00000430416.1:p.Pro17Leu
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro305Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

14-102698131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698131
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698131
    reference: chr 14
allele count: 8748
allele frequency: 7.263729511599715e-2
allele num: 120434
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1532C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+741C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.891C>T
  hgvsp: ENST00000522874.1:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+741C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+741C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.472C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1894C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.804C>T
  hgvsp: ENST00000524214.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2081C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.28C>T
  hgvsp: ENST00000521937.1:c.28C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+741C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+741C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+741C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+741C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.894C>T
  hgvsp: ENST00000361847.2:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+741C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+741C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1894C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+741C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.427C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+741C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser298Ser
num of homozygotes: 395
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/14-102698135-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698135
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698135
    reference: chr 14
allele count: 1
allele frequency: 8.315040244794785e-6
allele num: 120264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+737G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.397G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+737G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+737G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+737G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1877G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.627G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1532G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.800G>T
  hgvsp: ENSP00000428942.1:p.Gly267Val
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.468G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1528G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.928G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.890G>T
  hgvsp: ENSP00000355304.2:p.Gly297Val
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1890G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+737G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.24G>T
  hgvsp: ENSP00000430416.1:p.Gly9Val
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.423G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2077G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+737G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+737G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+737G>T
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly297Val
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/14-102698142-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698142
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698142
    reference: chr 14
allele count: 4
allele frequency: 3.329061038334138e-5
allele num: 120154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+730G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+730G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+730G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2070G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1525G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.793G>T
  hgvsp: ENSP00000428942.1:p.Ala265Ser
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.390G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.17G>T
  hgvsp: ENSP00000430416.1:p.Ala7Ser
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+730G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.883G>T
  hgvsp: ENSP00000355304.2:p.Ala295Ser
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.620G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1521G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.416G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+730G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.880G>T
  hgvsp: ENSP00000429469.1:p.Ala294Ser
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+730G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+730G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1883G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1870G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1883G>T
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala295Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

14-102698144-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698144
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698144
    reference: chr 14
allele count: 2
allele frequency: 1.665223472990075e-5
allele num: 120104
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+728G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+728G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.791G>A
  hgvsp: ENSP00000428942.1:p.Arg264Gln
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.388G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.15G>A
  hgvsp: ENSP00000430416.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1523G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1881G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+728G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.618G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.881G>A
  hgvsp: ENSP00000355304.2:p.Arg294Gln
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+728G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1868G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.414G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+728G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+728G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2068G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.878G>A
  hgvsp: ENSP00000429469.1:p.Arg293Gln
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1881G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1519G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+728G>A
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg294Gln
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-102698145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698145
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698145
    reference: chr 14
allele count: 3
allele frequency: 2.498625755834291e-5
allele num: 120066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1867C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+727C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+727C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+727C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.880C>T
  hgvsp: ENSP00000355304.2:p.Arg294Trp
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.413C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1522C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1518C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.790C>T
  hgvsp: ENSP00000428942.1:p.Arg264Trp
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+727C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2067C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+727C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.617C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+727C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+727C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+727C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.918C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1880C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+727C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.877C>T
  hgvsp: ENSP00000429469.1:p.Arg293Trp
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.14C>T
  hgvsp: ENSP00000430416.1:p.Arg6Trp
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg294Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

14-102698147-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698147
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698145
    reference: chr 14
allele count: 2
allele frequency: 1.666527789350887e-5
allele num: 120010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2063_2064delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.10_11delGA
  hgvsp: ENSP00000430416.1:p.Lys5AlafsTer23
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1518_1519delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+723_64+724delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+723_64+724delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+723_64+724delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+723_64+724delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1514_*1515delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.613_614delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+723_64+724delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.383_384delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.409_410delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.914_915delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+723_64+724delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.873_874delGA
  hgvsp: ENSP00000429469.1:p.Lys292AlafsTer23
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.876_877delGA
  hgvsp: ENSP00000355304.2:p.Lys293AlafsTer23
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.786_787delGA
  hgvsp: ENSP00000428942.1:p.Lys263AlafsTer23
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.454_455delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1863_1864delGA
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+723_504+724delGA
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys293AlafsTer23
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: TTC
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-102698148-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698148
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698147
    reference: chr 14
allele count: 1
allele frequency: 8.332777814812346e-6
allele num: 120008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1863delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+723delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1518delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.873delG
  hgvsp: ENSP00000429469.1:p.Lys292SerfsTer39
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.454delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2063delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.786delG
  hgvsp: ENSP00000428942.1:p.Lys263SerfsTer39
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000430416
  ensembl transcript: ENST00000521937
  gene symbol: MOK
  hgvsc: ENST00000521937.1:c.10delG
  hgvsp: ENSP00000430416.1:p.Lys5SerfsTer39
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.876delG
  hgvsp: ENSP00000355304.2:p.Lys293SerfsTer39
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+723delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+723delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1876delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+723delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.914delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.613delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1514delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.409delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.383delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+723delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+723delG
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1876delG
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys293SerfsTer39
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: TC
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

14-102698159-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698159
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698159
    reference: chr 14
allele count: 3
allele frequency: 2.505261048201223e-5
allele num: 119748
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+713G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-1G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+713G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+713G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+713G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-1G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-1G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.904G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-1G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+713G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+713G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-1G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-1G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+713G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-1G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+713G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1866G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-1G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1866G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+713G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-1G>A
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.867-1G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/14-102698161-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698161
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698161
    reference: chr 14
allele count: 3
allele frequency: 2.50685206230363e-5
allele num: 119672
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-3T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-3T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-3T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-3T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+711T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.374-3T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-3T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-3T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+711T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-3T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+711T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1864T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.902T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1864T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+711T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-3T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-3T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+711T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+711T>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+711T>G
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.867-3T>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

14-102698162-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698162
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698162
    reference: chr 14
allele count: 1
allele frequency: 8.357849692431131e-6
allele num: 119648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+710G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.374-4G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-4G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-4G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-4G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+710G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+710G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-4G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.901G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-4G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-4G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-4G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+710G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-4G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+710G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1863G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1863G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-4G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+710G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+710G>A
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.867-4G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

14-102698163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698163
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698163
    reference: chr 14
allele count: 9
allele frequency: 7.525586995785671e-5
allele num: 119592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-5C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-5C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1862C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-5C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.900C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-5C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-5C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+709C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+709C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+709C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-5C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.374-5C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+709C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1862C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-5C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-5C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-5C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+709C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-5C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+709C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.867-5C>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

14-102698166-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698166
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698166
    reference: chr 14
allele count: 2
allele frequency: 1.673276107290464e-5
allele num: 119526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-8C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-8C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+706C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+706C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-8C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-8C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-8C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+706C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+706C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+706C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-8C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+706C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-8C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.374-8C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-8C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-8C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.897C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-8C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+706C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1859C>A
  variant of: http://identifiers.org/hgnc/9833
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.867-8C>A
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

14-102698167-AAGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698167
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698164
    reference: chr 14
allele count: 1
allele frequency: 8.36638053645232e-6
allele num: 119526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+702_64+704delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+702_64+704delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-12_400-10delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1855_172+1857delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.893_895delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-12_445-10delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-12_*1505-10delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+702_64+704delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-12_867-10delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+702_64+704delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-12_864-10delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+702_504+704delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-12_777-10delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-12_604-10delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-12_2054-10delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+702_164+704delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+702_64+704delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+702_64+704delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+702_64+704delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+702_64+704delCCT
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-12_1854-10delCCT
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: AAGG
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

14-102698175-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698175
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698175
    reference: chr 14
allele count: 1
allele frequency: 8.382791804982731e-6
allele num: 119292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-17C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-17C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+697C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1850C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-17C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+697C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.374-17C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-17C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+697C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+697C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-17C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+697C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-17C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+697C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+697C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-17C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.888C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-17C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-17C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1850C>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-17C>A
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

14-102698181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698181
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698181
    reference: chr 14
allele count: 1
allele frequency: 8.394614015647561e-6
allele num: 119124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-23C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+691C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-23C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-23C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+691C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+691C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+691C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1844C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+691C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+691C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+691C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-23C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-23C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+691C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-23C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+691C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-23C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.882C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-23C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1844C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-23C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

14-102698187-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698187
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698187
    reference: chr 14
allele count: 1
allele frequency: 8.404915194405689e-6
allele num: 118978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+685C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+685C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+685C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+685C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+685C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.876C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-29C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-29C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.374-29C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+685C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+685C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-29C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+685C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-29C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-29C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-29C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-29C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1838C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+685C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-29C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-29C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

14-102698187-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698187
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698187
    reference: chr 14
allele count: 1
allele frequency: 8.404915194405689e-6
allele num: 118978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+685C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+685C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-29C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-29C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-29C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-29C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+685C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+685C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-29C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+685C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.876C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+685C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-29C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-29C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-29C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1838C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1838C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.374-29C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+685C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+685C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-29C>G
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

14-102698202-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698202
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698202
    reference: chr 14
allele count: 4
allele frequency: 3.382721060821325e-5
allele num: 118248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1823G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+670G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1823G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-44G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+670G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+670G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.374-44G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+670G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-44G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-44G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-44G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+670G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+670G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-44G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.861G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+670G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-44G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+670G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-44G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-44G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-44G>A
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

14-102698203-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698203
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698203
    reference: chr 14
allele count: 1
allele frequency: 8.463530646444471e-6
allele num: 118154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-45C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1822C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-45C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-45C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-45C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.860C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-45C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-45C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+669C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-45C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+669C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+669C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+669C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+669C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-45C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1822C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+669C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-45C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+669C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.374-45C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-45C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-102698208-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698208
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698208
    reference: chr 14
allele count: 4
allele frequency: 3.396047001290498e-5
allele num: 117784
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+664C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+664C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+664C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+664C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+664C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-50C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-50C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+664C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-50C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-50C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-50C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-50C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-50C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.855C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+664C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-50C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1817C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+664C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1817C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-50C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+664C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

http://identifiers.org/exac.variant/14-102698209-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698209
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698209
    reference: chr 14
allele count: 1
allele frequency: 8.505137102810097e-6
allele num: 117576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+663G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1816G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.400-51G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.867-51G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+663G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.374-51G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2054-51G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1854-51G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.864-51G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+663G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.777-51G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1505-51G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1509-51G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.604-51G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.854G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+663G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+663G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+663G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+663G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.445-51G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1816G>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-102698825-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698825
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698825
    reference: chr 14
allele count: 318
allele frequency: 2.7374619079593e-3
allele num: 116166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.603+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2053+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.866+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.399+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.238A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1504+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1508+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1200A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.373+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.863+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1853+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.776+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+47A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+47A>G
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

14-102698826-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698826
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698826
    reference: chr 14
allele count: 2
allele frequency: 1.721674155949245e-5
allele num: 116166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1508+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.237A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.776+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.373+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.603+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.863+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.866+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1504+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.399+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1853+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1199A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+46A>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1199A>G
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

14-102698829-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698829
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698829
    reference: chr 14
allele count: 2
allele frequency: 1.722920004824176e-5
allele num: 116082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.373+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.444+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.776+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1853+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1504+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1196G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.399+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.234G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.866+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1508+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.863+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.603+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2053+43G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+43G>A
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

14-102698832-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698832
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698832
    reference: chr 14
allele count: 1
allele frequency: 8.596234849136078e-6
allele num: 116330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.776+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.444+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1853+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1504+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.399+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2053+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.866+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.373+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.863+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.603+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.231C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1193C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+40C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+40C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-102698837-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698837
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698837
    reference: chr 14
allele count: 2
allele frequency: 1.717121417655442e-5
allele num: 116474
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.776+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.399+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.373+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2053+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1504+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1853+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1508+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.444+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.863+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.603+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.226A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+35A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.866+35A>C
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

14-102698838-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698838
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698838
    reference: chr 14
allele count: 2
allele frequency: 1.716355148207267e-5
allele num: 116526
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.863+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.603+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.399+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454203
  ensembl transcript: ENST00000522534
  gene symbol: MOK
  hgvsc: ENST00000522534.1:c.64+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.776+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1187C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1187C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1853+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2053+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.225C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.373+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.444+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1504+34C>G
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1508+34C>G
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-102698843-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698843
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698843
    reference: chr 14
allele count: 1
allele frequency: 8.559884955146204e-6
allele num: 116824
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.866+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.863+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1182A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1508+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1853+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000452978
  ensembl transcript: ENST00000524370
  gene symbol: MOK
  hgvsc: ENST00000524370.1:c.64+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.444+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.399+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1182A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.603+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.220A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.776+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+29A>C
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+29A>C
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-102698844-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698844
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698844
    reference: chr 14
allele count: 1
allele frequency: 8.558273282782466e-6
allele num: 116846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1181C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1504+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1181C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1508+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.373+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.603+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2053+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1853+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.866+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.399+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.776+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.863+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.219C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+28C>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.444+28C>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/14-102698848-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698848
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698848
    reference: chr 14
allele count: 1
allele frequency: 8.529512111907199e-6
allele num: 117240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1177G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.215G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.776+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1504+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.603+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.399+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.866+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520266
  gene symbol: MOK
  hgvsc: ENST00000520266.1:n.293+1177G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1853+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.373+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.444+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453224
  ensembl transcript: ENST00000517966
  gene symbol: MOK
  hgvsc: ENST00000517966.1:c.64+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1508+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+24G>T
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+24G>T
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
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: Other
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

14-102698848-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102698848
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 102698848
    reference: chr 14
allele count: 10
allele frequency: 8.5295121119072e-5
allele num: 117240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429469
  ensembl transcript: ENST00000522874
  gene symbol: MOK
  hgvsc: ENST00000522874.1:c.863+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000355304
  ensembl transcript: ENST00000361847
  gene symbol: MOK
  hgvsc: ENST00000361847.2:c.866+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453401
  ensembl transcript: ENST00000559138
  gene symbol: MOK
  hgvsc: ENST00000559138.1:c.64+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000524120
  gene symbol: MOK
  hgvsc: ENST00000524120.1:n.399+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000193029
  ensembl transcript: ENST00000193029
  gene symbol: MOK
  hgvsc: ENST00000193029.6:c.164+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453762
  ensembl transcript: ENST00000523231
  gene symbol: MOK
  hgvsc: ENST00000523231.1:c.64+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519477
  gene symbol: MOK
  hgvsc: ENST00000519477.1:n.373+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429672
  ensembl transcript: ENST00000519058
  gene symbol: MOK
  hgvsc: ENST00000519058.1:c.64+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000428942
  ensembl transcript: ENST00000524214
  gene symbol: MOK
  hgvsc: ENST00000524214.1:c.776+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000429348
  ensembl transcript: ENST00000521766
  gene symbol: MOK
  hgvsc: ENST00000521766.1:c.*1504+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000518686
  gene symbol: MOK
  hgvsc: ENST00000518686.1:n.2053+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000519569
  gene symbol: MOK
  hgvsc: ENST00000519569.1:n.1508+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520252
  gene symbol: MOK
  hgvsc: ENST00000520252.1:n.444+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000520046
  gene symbol: MOK
  hgvsc: ENST00000520046.1:n.603+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000521249
  gene symbol: MOK
  hgvsc: ENST00000521249.1:n.215G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000557823
  gene symbol: MOK
  hgvsc: ENST00000557823.1:n.172+1177G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453449
  ensembl transcript: ENST00000559838
  gene symbol: MOK
  hgvsc: ENST00000559838.1:c.504+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000454098
  ensembl transcript: ENST00000522867
  gene symbol: MOK
  hgvsc: ENST00000522867.1:c.64+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453799
  ensembl transcript: ENST00000522537
  gene symbol: MOK
  hgvsc: ENST00000522537.1:c.64+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl protein: ENSP00000453950
  ensembl transcript: ENST00000561150
  gene symbol: MOK
  hgvsc: ENST00000561150.1:c.64+24G>A
  variant of: http://identifiers.org/hgnc/9833
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080823
  ensembl transcript: ENST00000523485
  gene symbol: MOK
  hgvsc: ENST00000523485.1:n.1853+24G>A
  variant of: http://identifiers.org/hgnc/9833
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: C

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000428942
ensembl transcript: ENST00000524214
gene symbol: MOK
hgvsc: ENST00000524214.1:c.891+41C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453799
ensembl transcript: ENST00000522537
gene symbol: MOK
hgvsc: ENST00000522537.1:c.64+869C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000430416
ensembl transcript: ENST00000521937
gene symbol: MOK
hgvsc: ENST00000521937.1:c.115+41C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+869C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 1220
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3892
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7504
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 6533
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5165
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 354
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 474
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3153
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1089
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5984
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6153
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5350
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6370
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2627
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1720
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 597
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 535
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1760
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3385
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31114
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3103
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3190
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1778
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3976
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9353
bin: 6.25e1
variant carriers: 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: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.011322572874006e-5
allele num: 66416
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.385e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.01e0

VQSLOD
type: SiteQuality
SIO_000300: 5.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.22e-1

DP
type: SiteQuality
SIO_000300: 3.338429e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.488+38A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453799
ensembl transcript: ENST00000522537
gene symbol: MOK
hgvsc: ENST00000522537.1:c.64+866A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000428942
ensembl transcript: ENST00000524214
gene symbol: MOK
hgvsc: ENST00000524214.1:c.891+38A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+866A>G
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 2627
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 597
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5350
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3557
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 836
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 535
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3892
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1720
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5255
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6151
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6370
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5994
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 979
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6536
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 473
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7502
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1780
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10011
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 267
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31110
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1764
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4020
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3106
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3194
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3386
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66434
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16074
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

DP
type: SiteQuality
SIO_000300: 3.341595e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -9.23e-1

MQ
type: SiteQuality
SIO_000300: 5.785e1

VQSLOD
type: SiteQuality
SIO_000300: 2.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.759e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+861A>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520252
gene symbol: MOK
hgvsc: ENST00000520252.1:n.559+33A>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+861A>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.488+33A>C
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 3892
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3848
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 341
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6535
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2627
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1720
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6370
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5350
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7502
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 832
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6012
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5387
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 535
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 473
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 597
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 560
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6150
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 348
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31111
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10358
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3116
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1781
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1762
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3201
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3392
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505072092953252e-5
allele num: 66442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.561e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-1

FS
type: SiteQuality
SIO_000300: 8.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

QD
type: SiteQuality
SIO_000300: 1.288e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.01e-1

DP
type: SiteQuality
SIO_000300: 3.345501e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429469
ensembl transcript: ENST00000522874
gene symbol: MOK
hgvsc: ENST00000522874.1:c.978+29G>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000430416
ensembl transcript: ENST00000521937
gene symbol: MOK
hgvsc: ENST00000521937.1:c.115+29G>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+2010G>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519569
gene symbol: MOK
hgvsc: ENST00000519569.1:n.1623+29G>C
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 3905
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 811
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5350
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 597
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 328
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7502
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 5513
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6153
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3892
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2627
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 535
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 473
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1720
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6370
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6536
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6039
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 711
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10384
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 176
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1780
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3201
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3126
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31110
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3394
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4039
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505661286437003e-5
allele num: 66416
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.414e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.18e-1

FS
type: SiteQuality
SIO_000300: 3.505e0

DP
type: SiteQuality
SIO_000300: 3.348279e6

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.983e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000523485
gene symbol: MOK
hgvsc: ENST00000523485.1:n.1968+22G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000428942
ensembl transcript: ENST00000524214
gene symbol: MOK
hgvsc: ENST00000524214.1:c.891+22G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000518686
gene symbol: MOK
hgvsc: ENST00000518686.1:n.2168+22G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.488+22G>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 479
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6538
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6370
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6156
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 304
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5658
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 811
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4171
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5350
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7502
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 597
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6069
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 534
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 472
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3892
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2628
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1720
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1788
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31111
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4076
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10875
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 225
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3215
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3133
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3400
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504664459825459e-5
allele num: 66460
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.235941169200346e-4
allele num: 16182
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.272e0

QD
type: SiteQuality
SIO_000300: 1.491e1

FS
type: SiteQuality
SIO_000300: 2.182e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.320000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.353379e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.89e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429348
ensembl transcript: ENST00000521766
gene symbol: MOK
hgvsc: ENST00000521766.1:c.*1619+21C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000430416
ensembl transcript: ENST00000521937
gene symbol: MOK
hgvsc: ENST00000521937.1:c.115+21C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+849C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519569
gene symbol: MOK
hgvsc: ENST00000519569.1:n.1623+21C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 7501
bin: 9.75e1
variant carriers: 6

GenotypeDepth
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2630
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 418
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1720
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 259
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6154
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5670
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6077
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6370
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4272
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5350
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 293
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3892
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6537
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 596
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 811
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4092
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31112
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3134
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1790
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11048
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 8.25e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504483360414034e-5
allele num: 66468
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.849568434032059e-4
allele num: 16220
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.954e1

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 1.163e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

FS
type: SiteQuality
SIO_000300: 1.432e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

DP
type: SiteQuality
SIO_000300: 3.354201e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+844G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000193029
ensembl transcript: ENST00000193029
gene symbol: MOK
hgvsc: ENST00000193029.6:c.164+844G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+844G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453799
ensembl transcript: ENST00000522537
gene symbol: MOK
hgvsc: ENST00000522537.1:c.64+844G>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 6110
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5773
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1720
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6540
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 811
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3892
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4389
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 287
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 596
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5352
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7497
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 6370
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6159
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2629
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31114
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 3403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3234
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4118
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11243
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3136
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008695128922586e-5
allele num: 66474
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.92789666473877e-4
allele num: 10374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

FS
type: SiteQuality
SIO_000300: 2.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.52e-1

DP
type: SiteQuality
SIO_000300: 3.357227e6

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.156e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.488+16G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519569
gene symbol: MOK
hgvsc: ENST00000519569.1:n.1623+16G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1997G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+844G>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 2629
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 811
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6110
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5352
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3892
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 287
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6370
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7497
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 4389
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6540
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1720
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6159
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 596
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5773
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11243
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4118
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3234
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3136
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31114
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.51304269338388e-5
allele num: 66474
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

FS
type: SiteQuality
SIO_000300: 2.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.52e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

QD
type: SiteQuality
SIO_000300: 1.156e1

DP
type: SiteQuality
SIO_000300: 3.357227e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+843C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000518686
gene symbol: MOK
hgvsc: ENST00000518686.1:n.2168+15C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1996C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453799
ensembl transcript: ENST00000522537
gene symbol: MOK
hgvsc: ENST00000522537.1:c.64+843C>T
variant of: http://identifiers.org/hgnc/9833

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

GenotypeDepth
all individuals: 255
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7492
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1720
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6370
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5804
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5353
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4415
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2629
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6112
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 247
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3893
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 596
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 811
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6540
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4134
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3229
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31110
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 97
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11348
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3142
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3405
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1799
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007790176557283e-5
allele num: 66494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.37e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 3.357339e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

FS
type: SiteQuality
SIO_000300: 9.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e0

QD
type: SiteQuality
SIO_000300: 1.128e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453799
ensembl transcript: ENST00000522537
gene symbol: MOK
hgvsc: ENST00000522537.1:c.64+838G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1991G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520252
gene symbol: MOK
hgvsc: ENST00000520252.1:n.559+10G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+838G>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 3916
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 489
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 204
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1086
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6102
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 279
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2631
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5618
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3918
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1703
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6313
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5417
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6699
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6477
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 759
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8390
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1743
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3120
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10853
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1719
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3353
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32401
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3015
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.116956202593589e-5
allele num: 16348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.254e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.996e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.05e-2

QD
type: SiteQuality
SIO_000300: 1.431e1

VQSLOD
type: SiteQuality
SIO_000300: 4.66e0

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

DP
type: SiteQuality
SIO_000300: 4.222295e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000518686
gene symbol: MOK
hgvsc: ENST00000518686.1:n.2168+10G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520252
gene symbol: MOK
hgvsc: ENST00000520252.1:n.559+10G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+838G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+838G>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 6313
bin: 3.75e1
variant carriers: 232

GenotypeDepth
all individuals: 373
bin: 8.75e1
variant carriers: 25

GenotypeDepth
all individuals: 759
bin: 7.75e1
variant carriers: 52

GenotypeDepth
all individuals: 6699
bin: 4.25e1
variant carriers: 207

GenotypeDepth
all individuals: 6102
bin: 3.25e1
variant carriers: 177

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

GenotypeDepth
all individuals: 186
bin: 1.25e1
variant carriers: 21

GenotypeDepth
all individuals: 3916
bin: 5.75e1
variant carriers: 87

GenotypeDepth
all individuals: 3918
bin: 2.25e1
variant carriers: 82

GenotypeDepth
all individuals: 6477
bin: 4.75e1
variant carriers: 166

GenotypeDepth
all individuals: 1086
bin: 7.25e1
variant carriers: 32

GenotypeDepth
all individuals: 489
bin: 8.25e1
variant carriers: 32

GenotypeDepth
all individuals: 5618
bin: 2.75e1
variant carriers: 137

GenotypeDepth
all individuals: 204
bin: 7.5e0
variant carriers: 6

GenotypeDepth
all individuals: 5417
bin: 5.25e1
variant carriers: 134

GenotypeDepth
all individuals: 279
bin: 9.25e1
variant carriers: 23

GenotypeDepth
all individuals: 1703
bin: 6.75e1
variant carriers: 45

GenotypeDepth
all individuals: 2631
bin: 6.25e1
variant carriers: 59

GenotypeDepth
all individuals: 141
bin: 1.75e1
variant carriers: 41

GenotypeDepth
all individuals: 8390
bin: 9.75e1
variant carriers: 7182

GenotypeQuality
all individuals: 3353
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 59
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10853
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3120
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1719
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 254
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32401
bin: 9.75e1
variant carriers: 8713

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3015
bin: 7.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 1743
bin: 8.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 5586
allele frequency: 8.396717073024081e-2
allele num: 66526
num of homozygotes: 237

Other
type: Population
allele count: 61
allele frequency: 6.747787610619468e-2
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 478
allele frequency: 7.227094042939219e-2
allele num: 6614
num of homozygotes: 18

African
type: Population
allele count: 655
allele frequency: 6.317515432098765e-2
allele num: 10368
num of homozygotes: 28

Latino
type: Population
allele count: 441
allele frequency: 3.814218993253762e-2
allele num: 11562
num of homozygotes: 11

South Asian
type: Population
allele count: 1929
allele frequency: 1.179960851480303e-1
allele num: 16348
num of homozygotes: 130

East Asian
type: Population
allele count: 8
allele frequency: 9.248554913294797e-4
allele num: 8650
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.66e0

QD
type: SiteQuality
SIO_000300: 1.431e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

DP
type: SiteQuality
SIO_000300: 4.222295e6

FS
type: SiteQuality
SIO_000300: 1.254e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.05e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.996e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000430416
ensembl transcript: ENST00000521937
gene symbol: MOK
hgvsc: ENST00000521937.1:c.115+9C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453799
ensembl transcript: ENST00000522537
gene symbol: MOK
hgvsc: ENST00000522537.1:c.64+837C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+837C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1990C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 500
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6135
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8028
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 2651
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1720
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3970
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1098
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6325
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6546
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3934
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6706
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5455
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 756
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5681
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11113
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3440
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 266
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1799
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4034
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31682
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3212
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3084
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.510328652614487e-5
allele num: 66514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 1.205e0

QD
type: SiteQuality
SIO_000300: 1.314e1

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: 9.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 3.773706e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+835delA
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429348
ensembl transcript: ENST00000521766
gene symbol: MOK
hgvsc: ENST00000521766.1:c.*1619+7delA
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+835delA
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000193029
ensembl transcript: ENST00000193029
gene symbol: MOK
hgvsc: ENST00000193029.6:c.164+835delA
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+835delA
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 6709
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1098
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5699
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 198
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6136
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2651
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5455
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3935
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 170
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 119
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1720
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6546
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3965
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 756
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8027
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 500
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6327
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31683
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3078
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4040
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3212
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11135
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1760
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.469010175763182e-4
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.12e0

QD
type: SiteQuality
SIO_000300: 1.576e1

FS
type: SiteQuality
SIO_000300: 5.629999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.003e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

DP
type: SiteQuality
SIO_000300: 3.773955e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453449
ensembl transcript: ENST00000559838
gene symbol: MOK
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453224
ensembl transcript: ENST00000517966
gene symbol: MOK
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 6325
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3962
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3935
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5756
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1098
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8025
bin: 9.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 5455
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 500
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6706
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6548
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 756
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6132
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1721
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2651
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3209
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11205
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4023
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3083
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31680
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503397678753984e-5
allele num: 66516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
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: 8646
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.774062e6

MQ
type: SiteQuality
SIO_000300: 5.394e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 2.69e0

MQRankSum
type: SiteQuality
SIO_000300: -9.949999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-2

FS
type: SiteQuality
SIO_000300: 8.202e0

VQSLOD
type: SiteQuality
SIO_000300: -1.638e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+810C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+810C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1963C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+810C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+810C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 158
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6707
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 756
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1721
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6132
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5749
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5455
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3935
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3963
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6548
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6324
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8025
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 500
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2651
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1098
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11197
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3083
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1763
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 279
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1805
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4022
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31680
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3209
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503488092374308e-5
allele num: 66512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.408e0

VQSLOD
type: SiteQuality
SIO_000300: -1.794e0

DP
type: SiteQuality
SIO_000300: 3.774033e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.694e0

MQRankSum
type: SiteQuality
SIO_000300: 8.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.345e0

FS
type: SiteQuality
SIO_000300: 1.788e0

QD
type: SiteQuality
SIO_000300: 1.138e1

MQ
type: SiteQuality
SIO_000300: 5.952e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453449
ensembl transcript: ENST00000559838
gene symbol: MOK
hgvsc: ENST00000559838.1:c.504+803A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1956A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000193029
ensembl transcript: ENST00000193029
gene symbol: MOK
hgvsc: ENST00000193029.6:c.164+803A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+803A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453224
ensembl transcript: ENST00000517966
gene symbol: MOK
hgvsc: ENST00000517966.1:c.64+803A>G
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 6127
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6708
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3956
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5455
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6551
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1097
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1721
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 500
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 756
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3935
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5738
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6326
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8022
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2651
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4021
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11185
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1761
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3078
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 289
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31676
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1803
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
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: 10284
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503578516870151e-5
allele num: 66508
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.775633e6

VQSLOD
type: SiteQuality
SIO_000300: -1.339e0

QD
type: SiteQuality
SIO_000300: 1.828e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.1023e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.49e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+801C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429469
ensembl transcript: ENST00000522874
gene symbol: MOK
hgvsc: ENST00000522874.1:c.951C>G
hgvsp: ENSP00000429469.1:p.Cys317Trp
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+801C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+801C>G
variant of: http://identifiers.org/hgnc/9833

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

GenotypeDepth
all individuals: 381
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2651
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5734
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 500
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5455
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6708
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 756
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8022
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3935
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1721
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3959
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6129
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6327
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6550
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1097
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4019
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3077
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3208
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1761
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11201
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1803
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31675
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
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: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.304e0

VQSLOD
type: SiteQuality
SIO_000300: 7.7e-1

FS
type: SiteQuality
SIO_000300: 1.144e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.86e-1

DP
type: SiteQuality
SIO_000300: 3.775862e6

QD
type: SiteQuality
SIO_000300: 1.186e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+793A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+793A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.453A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+793A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453449
ensembl transcript: ENST00000559838
gene symbol: MOK
hgvsc: ENST00000559838.1:c.504+793A>G
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 6314
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6700
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1722
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6126
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3908
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 757
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8086
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6546
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1100
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 233
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2648
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5452
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3936
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 497
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5731
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 376
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 1.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 311
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3430
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3075
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4012
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11151
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3202
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31748
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
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: 8638
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.891e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

DP
type: SiteQuality
SIO_000300: 3.831136e6

MQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.64e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000557823
gene symbol: MOK
hgvsc: ENST00000557823.1:n.172+1945_172+1946insTC
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000518686
gene symbol: MOK
hgvsc: ENST00000518686.1:n.2132_2133insTC
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+792_64+793insTC
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+792_64+793insTC
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 5452
bin: 5.25e1
variant carriers: 3

GenotypeDepth
all individuals: 3908
bin: 2.25e1
variant carriers: 4

GenotypeDepth
all individuals: 6546
bin: 4.75e1
variant carriers: 3

GenotypeDepth
all individuals: 8086
bin: 9.75e1
variant carriers: 356

GenotypeDepth
all individuals: 6126
bin: 3.25e1
variant carriers: 5

GenotypeDepth
all individuals: 233
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 1.25e1
variant carriers: 6

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

GenotypeDepth
all individuals: 6700
bin: 4.25e1
variant carriers: 7

GenotypeDepth
all individuals: 3936
bin: 5.75e1
variant carriers: 4

GenotypeDepth
all individuals: 87
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1100
bin: 7.25e1
variant carriers: 9

GenotypeDepth
all individuals: 1722
bin: 6.75e1
variant carriers: 8

GenotypeDepth
all individuals: 497
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 5731
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 6314
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2648
bin: 6.25e1
variant carriers: 6

GenotypeDepth
all individuals: 376
bin: 8.75e1
variant carriers: 5

GenotypeDepth
all individuals: 301
bin: 9.25e1
variant carriers: 4

GenotypeDepth
all individuals: 757
bin: 7.75e1
variant carriers: 7

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3202
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4012
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 311
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3430
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3075
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31748
bin: 9.75e1
variant carriers: 434

GenotypeQuality
all individuals: 11151
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1801
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.557006196979724e-4
allele num: 66484
num of homozygotes: 0

African
type: Population
allele count: 386
allele frequency: 3.749757140081601e-2
allele num: 10294
num of homozygotes: 12

East Asian
type: Population
allele count: 6
allele frequency: 6.946052326927529e-4
allele num: 8638
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.50546780072904e-4
allele num: 16460
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 23
allele frequency: 1.993067590987868e-3
allele num: 11540
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.53e-1

DP
type: SiteQuality
SIO_000300: 3.831136e6

VQSLOD
type: SiteQuality
SIO_000300: 4.73e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.64e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

QD
type: SiteQuality
SIO_000300: 1.891e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+781G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+781G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000521249
gene symbol: MOK
hgvsc: ENST00000521249.1:n.972G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000557823
gene symbol: MOK
hgvsc: ENST00000557823.1:n.172+1934G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+781G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453449
ensembl transcript: ENST00000559838
gene symbol: MOK
hgvsc: ENST00000559838.1:c.504+781G>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 202
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5481
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6376
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3957
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3890
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 755
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5784
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6590
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2659
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1104
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 272
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6731
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6183
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1723
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 499
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7740
bin: 9.75e1
variant carriers: 16

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

GenotypeQuality
all individuals: 3452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3228
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31477
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11222
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4055
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3108
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.107100930134554e-4
allele num: 66442
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.537205081669691e-4
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.848e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

DP
type: SiteQuality
SIO_000300: 3.743262e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+779C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453224
ensembl transcript: ENST00000517966
gene symbol: MOK
hgvsc: ENST00000517966.1:c.64+779C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+779C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1932C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.439C>T
variant of: http://identifiers.org/hgnc/9833

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

GenotypeDepth
all individuals: 1104
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 498
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6382
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6734
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2661
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1724
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3847
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7724
bin: 9.75e1
variant carriers: 9

GenotypeDepth
all individuals: 5776
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6594
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6192
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5481
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 755
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3957
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31466
bin: 9.75e1
variant carriers: 9

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

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3108
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4043
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1776
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.754194303550527e-5
allele num: 10252
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.022645145748013e-5
allele num: 66416
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.733402669440111e-4
allele num: 11538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.88e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.265e1

MQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

DP
type: SiteQuality
SIO_000300: 3.740236e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+778C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+778C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520252
gene symbol: MOK
hgvsc: ENST00000520252.1:n.509C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453799
ensembl transcript: ENST00000522537
gene symbol: MOK
hgvsc: ENST00000522537.1:c.64+778C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519569
gene symbol: MOK
hgvsc: ENST00000519569.1:n.1573C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+778C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 6190
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1104
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1725
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5481
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 754
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2662
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6735
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6381
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3957
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3850
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 498
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7717
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 6595
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5780
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4045
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3453
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11172
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3110
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3229
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31461
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 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: 8632
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.9032006245121e-4
allele num: 10248
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.61e-1

QD
type: SiteQuality
SIO_000300: 1.373e1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.704e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

FS
type: SiteQuality
SIO_000300: 1.137e0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 3.738615e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453449
ensembl transcript: ENST00000559838
gene symbol: MOK
hgvsc: ENST00000559838.1:c.504+770C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000557823
gene symbol: MOK
hgvsc: ENST00000557823.1:n.172+1923C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1923C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+770C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+770C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+770C>G
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6735
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2664
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5482
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6190
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1724
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 315
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7714
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6595
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6381
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5771
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1104
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3830
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 754
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 498
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3957
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4039
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3453
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1774
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11160
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3229
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31460
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3110
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66382
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.216397031991242e-4
allele num: 16442
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.988e1

VQSLOD
type: SiteQuality
SIO_000300: -4.29e-2

DP
type: SiteQuality
SIO_000300: 3.737416e6

QD
type: SiteQuality
SIO_000300: 1.147e1

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.347e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+769C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000521249
gene symbol: MOK
hgvsc: ENST00000521249.1:n.960C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+769C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+769C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453449
ensembl transcript: ENST00000559838
gene symbol: MOK
hgvsc: ENST00000559838.1:c.504+769C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1922C>G
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 316
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 221
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6190
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 498
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3830
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 755
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7713
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2664
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5482
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6736
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6381
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1724
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3957
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5771
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1104
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6595
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1774
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4036
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11166
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31460
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3229
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3109
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3453
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66378
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
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: 8628
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.873e1

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.84e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.356e0

QD
type: SiteQuality
SIO_000300: 8.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.737227e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.303e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+762G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429348
ensembl transcript: ENST00000521766
gene symbol: MOK
hgvsc: ENST00000521766.1:c.*1553G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+762G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000524120
gene symbol: MOK
hgvsc: ENST00000524120.1:n.448G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519569
gene symbol: MOK
hgvsc: ENST00000519569.1:n.1557G>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 5763
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1724
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6736
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6189
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6381
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3957
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 230
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5482
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3802
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6593
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2664
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7713
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 498
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 754
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 456
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3228
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3453
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11150
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31458
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3107
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.769441187964049e-5
allele num: 10236
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.736487e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.724e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.261e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 4.83e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519569
gene symbol: MOK
hgvsc: ENST00000519569.1:n.1556C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000193029
ensembl transcript: ENST00000193029
gene symbol: MOK
hgvsc: ENST00000193029.6:c.164+761C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+761C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+761C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+761C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 345
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 498
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5765
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1724
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6593
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1104
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 234
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5482
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6737
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 754
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2664
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6380
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6190
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3795
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3957
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7713
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31458
bin: 9.75e1
variant carriers: 10

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

GenotypeQuality
all individuals: 3453
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3107
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.673026886383348e-5
allele num: 11530
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.217285453438831e-4
allele num: 16430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.318571759795966e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.030453791647822e-5
allele num: 66330
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.46e0

MQRankSum
type: SiteQuality
SIO_000300: 5.47e-1

DP
type: SiteQuality
SIO_000300: 3.737141e6

QD
type: SiteQuality
SIO_000300: 1.473e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.76e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.85e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000523485
gene symbol: MOK
hgvsc: ENST00000523485.1:n.1881C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520046
gene symbol: MOK
hgvsc: ENST00000520046.1:n.631C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519569
gene symbol: MOK
hgvsc: ENST00000519569.1:n.1536C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.401C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000521249
gene symbol: MOK
hgvsc: ENST00000521249.1:n.932C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 302
bin: 1.25e1
variant carriers: 43

GenotypeDepth
all individuals: 5646
bin: 2.75e1
variant carriers: 37

GenotypeDepth
all individuals: 583
bin: 8.25e1
variant carriers: 123

GenotypeDepth
all individuals: 6480
bin: 4.75e1
variant carriers: 87

GenotypeDepth
all individuals: 3629
bin: 2.25e1
variant carriers: 49

GenotypeDepth
all individuals: 438
bin: 7.5e0
variant carriers: 13

GenotypeDepth
all individuals: 436
bin: 8.75e1
variant carriers: 94

GenotypeDepth
all individuals: 2750
bin: 6.25e1
variant carriers: 156

GenotypeDepth
all individuals: 1196
bin: 7.25e1
variant carriers: 126

GenotypeDepth
all individuals: 5456
bin: 5.25e1
variant carriers: 106

GenotypeDepth
all individuals: 3992
bin: 5.75e1
variant carriers: 125

GenotypeDepth
all individuals: 6056
bin: 3.25e1
variant carriers: 41

GenotypeDepth
all individuals: 6618
bin: 4.25e1
variant carriers: 68

GenotypeDepth
all individuals: 836
bin: 7.75e1
variant carriers: 123

GenotypeDepth
all individuals: 111
bin: 1.75e1
variant carriers: 47

GenotypeDepth
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7767
bin: 9.75e1
variant carriers: 6862

GenotypeDepth
all individuals: 1821
bin: 6.75e1
variant carriers: 149

GenotypeDepth
all individuals: 6225
bin: 3.75e1
variant carriers: 42

GenotypeDepth
all individuals: 329
bin: 9.25e1
variant carriers: 78

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3160
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 3953
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1728
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3055
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1766
bin: 8.75e1
variant carriers: 8

GenotypeQuality
all individuals: 3386
bin: 9.25e1
variant carriers: 6

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 10874
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 31946
bin: 9.75e1
variant carriers: 8334

European (Non-Finnish)
type: Population
allele count: 5565
allele frequency: 8.405836505347108e-2
allele num: 66204
num of homozygotes: 236

African
type: Population
allele count: 288
allele frequency: 2.82574568288854e-2
allele num: 10192
num of homozygotes: 1

South Asian
type: Population
allele count: 1927
allele frequency: 1.175e-1
allele num: 16400
num of homozygotes: 129

European (Finnish)
type: Population
allele count: 478
allele frequency: 7.229280096793708e-2
allele num: 6612
num of homozygotes: 18

Other
type: Population
allele count: 59
allele frequency: 6.570155902004454e-2
allele num: 898
num of homozygotes: 0

Latino
type: Population
allele count: 423
allele frequency: 3.671875e-2
allele num: 11520
num of homozygotes: 11

East Asian
type: Population
allele count: 8
allele frequency: 9.293680297397769e-4
allele num: 8608
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.712642e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.15e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

QD
type: SiteQuality
SIO_000300: 1.502e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.122e0

FS
type: SiteQuality
SIO_000300: 1.551e0

VQSLOD
type: SiteQuality
SIO_000300: 4.67e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+737G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+737G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000557823
gene symbol: MOK
hgvsc: ENST00000557823.1:n.172+1890G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429469
ensembl transcript: ENST00000522874
gene symbol: MOK
hgvsc: ENST00000522874.1:c.887G>T
hgvsp: ENSP00000429469.1:p.Gly296Val
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+737G>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4538
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7354
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3842
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 523
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3108
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7488
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7048
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 834
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1989
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7003
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6688
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6222
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 554
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1069
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1288
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4554
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3550
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3618
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27605
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51267622678042e-5
allele num: 66108
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.761e0

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.922e1

QD
type: SiteQuality
SIO_000300: 1.372e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.04e-1

DP
type: SiteQuality
SIO_000300: 2.726441e6

FS
type: SiteQuality
SIO_000300: 5.828e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.432e0

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453224
ensembl transcript: ENST00000517966
gene symbol: MOK
hgvsc: ENST00000517966.1:c.64+730G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000521249
gene symbol: MOK
hgvsc: ENST00000521249.1:n.921G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+730G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000193029
ensembl transcript: ENST00000193029
gene symbol: MOK
hgvsc: ENST00000193029.6:c.164+730G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+730G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520252
gene symbol: MOK
hgvsc: ENST00000520252.1:n.461G>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 555
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 390
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6629
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1288
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 835
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3817
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6220
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6993
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7484
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4538
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7040
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1989
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7355
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1069
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1968
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3549
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12416
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3615
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4524
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3874
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27607
bin: 9.75e1
variant carriers: 4

South Asian
type: Population
allele count: 4
allele frequency: 2.448579823702253e-4
allele num: 16336
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 9.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.19e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

DP
type: SiteQuality
SIO_000300: 2.72444e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.66e0

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+728G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+728G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453449
ensembl transcript: ENST00000559838
gene symbol: MOK
hgvsc: ENST00000559838.1:c.504+728G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520252
gene symbol: MOK
hgvsc: ENST00000520252.1:n.459G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000193029
ensembl transcript: ENST00000193029
gene symbol: MOK
hgvsc: ENST00000193029.6:c.164+728G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000521249
gene symbol: MOK
hgvsc: ENST00000521249.1:n.919G>A
variant of: http://identifiers.org/hgnc/9833

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

GenotypeDepth
all individuals: 1988
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7032
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7354
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 577
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7480
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6620
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6990
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 421
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4538
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1288
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 835
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3788
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6220
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3108
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1067
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 12358
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27603
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3550
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.02929326588107e-5
allele num: 66022
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

DP
type: SiteQuality
SIO_000300: 2.723086e6

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

QD
type: SiteQuality
SIO_000300: 1.337e1

VQSLOD
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.67e0

FS
type: SiteQuality
SIO_000300: 7.909e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+727C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+727C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520252
gene symbol: MOK
hgvsc: ENST00000520252.1:n.458C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1880C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.387C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6984
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 589
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7478
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1065
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 834
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1988
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4538
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3776
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6220
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7025
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7355
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1288
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6625
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27600
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 97
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3548
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3615
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12335
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4515
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.029843963035904e-5
allele num: 66010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
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: 11496
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: 10142
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164144353899884e-4
allele num: 8590
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.58e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.674e0

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

DP
type: SiteQuality
SIO_000300: 2.722321e6

QD
type: SiteQuality
SIO_000300: 1.296e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+723_64+724delGA
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1876_293+1877delGA
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000193029
ensembl transcript: ENST00000193029
gene symbol: MOK
hgvsc: ENST00000193029.6:c.164+723_164+724delGA
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+723_64+724delGA
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000557823
gene symbol: MOK
hgvsc: ENST00000557823.1:n.172+1876_172+1877delGA
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+723_64+724delGA
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 4538
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6586
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6220
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7355
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1288
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7479
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 618
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 401
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7021
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 296
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 834
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6963
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3744
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1061
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1988
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27599
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4500
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12256
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3874
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1958
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3612
bin: 8.25e1
variant carriers: 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: 11486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65984
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.226391954868776e-4
allele num: 16308
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 6.114e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.01e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.42e-1

DP
type: SiteQuality
SIO_000300: 2.720438e6

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

MQRankSum
type: SiteQuality
SIO_000300: -1.166e0

QD
type: SiteQuality
SIO_000300: 2.628e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+723delG
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000193029
ensembl transcript: ENST00000193029
gene symbol: MOK
hgvsc: ENST00000193029.6:c.164+723delG
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+723delG
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+723delG
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453799
ensembl transcript: ENST00000522537
gene symbol: MOK
hgvsc: ENST00000522537.1:c.64+723delG
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6964
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3749
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 619
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1988
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6220
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1288
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4538
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 472
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7479
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6581
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7355
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7020
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 401
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1061
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 834
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27598
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3874
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4496
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3545
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3612
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12278
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.869719699960521e-5
allele num: 10132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65984
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
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: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16306
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.86e0

MQ
type: SiteQuality
SIO_000300: 6.049e1

FS
type: SiteQuality
SIO_000300: 5.477e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

QD
type: SiteQuality
SIO_000300: 1.406e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.397e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.147e0

DP
type: SiteQuality
SIO_000300: 2.720317e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453799
ensembl transcript: ENST00000522537
gene symbol: MOK
hgvsc: ENST00000522537.1:c.64+713G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: splice_acceptor_variant
consequence: non_coding_transcript_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.374-1G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: splice_acceptor_variant
consequence: non_coding_transcript_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000523485
gene symbol: MOK
hgvsc: ENST00000523485.1:n.1854-1G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+713G>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 6997
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3583
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6428
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7354
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 686
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 834
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1988
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 131
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 707
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4538
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6220
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1061
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 6876
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1288
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7477
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3529
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3874
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4438
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1943
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11885
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27594
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.554563672800146e-5
allele num: 65868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 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: 16232
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.25e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.066e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.544e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

FS
type: SiteQuality
SIO_000300: 4.411e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e-2

DP
type: SiteQuality
SIO_000300: 2.713335e6

QD
type: SiteQuality
SIO_000300: 1.978e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520252
gene symbol: MOK
hgvsc: ENST00000520252.1:n.445-3T>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+711T>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+711T>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+711T>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453449
ensembl transcript: ENST00000559838
gene symbol: MOK
hgvsc: ENST00000559838.1:c.504+711T>G
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 706
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 209
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7354
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6219
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4539
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7475
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6850
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1058
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 6363
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3531
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6988
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1989
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 834
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1288
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27593
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3525
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11699
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 186
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3603
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65838
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

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

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

African
type: Population
allele count: 3
allele frequency: 2.975009916699722e-4
allele num: 10084
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 2.71068e6

VQSLOD
type: SiteQuality
SIO_000300: 5.590000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.49e0

QD
type: SiteQuality
SIO_000300: 1.809e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+710G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000428942
ensembl transcript: ENST00000524214
gene symbol: MOK
hgvsc: ENST00000524214.1:c.777-4G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453224
ensembl transcript: ENST00000517966
gene symbol: MOK
hgvsc: ENST00000517966.1:c.64+710G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453799
ensembl transcript: ENST00000522537
gene symbol: MOK
hgvsc: ENST00000522537.1:c.64+710G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000193029
ensembl transcript: ENST00000193029
gene symbol: MOK
hgvsc: ENST00000193029.6:c.164+710G>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 7478
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1055
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1288
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3529
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7355
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6219
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 834
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 712
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 797
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6990
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 202
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6359
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1989
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6851
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4540
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4420
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3604
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1934
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3525
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11723
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27591
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519110408944522e-5
allele num: 65828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.676e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.48e-1

DP
type: SiteQuality
SIO_000300: 2.710414e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.555e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453449
ensembl transcript: ENST00000559838
gene symbol: MOK
hgvsc: ENST00000559838.1:c.504+709C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+709C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+709C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+709C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+709C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6986
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 818
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7476
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6823
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 834
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 212
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7353
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3525
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 716
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6350
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1990
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1054
bin: 9.75e1
variant carriers: 6

GenotypeDepth
all individuals: 4540
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6219
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1289
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3521
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 197
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3599
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27588
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 4413
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11706
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.968253968253968e-4
allele num: 10080
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.599015167634275e-5
allele num: 65798
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16184
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.70926e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.206e0

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.43e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.459e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+706C>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+706C>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453224
ensembl transcript: ENST00000517966
gene symbol: MOK
hgvsc: ENST00000517966.1:c.64+706C>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1859C>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+706C>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 3400
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 950
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4539
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7473
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 734
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7353
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6796
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6285
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6987
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1989
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1049
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1287
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6214
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 399
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4394
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3515
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3601
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11484
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27576
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1982
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52031135976648e-5
allele num: 65776
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
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: 6.183527083848628e-5
allele num: 16172
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.701e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 8.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.705223e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.348e0

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+702_64+704delCCT
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519569
gene symbol: MOK
hgvsc: ENST00000519569.1:n.1509-12_1509-10delCCT
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.374-12_374-10delCCT
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1855_293+1857delCCT
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 7353
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7473
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1287
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6791
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6987
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 265
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 399
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3407
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1989
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 738
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 950
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 195
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6214
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4539
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6281
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1049
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3601
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27574
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3514
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4394
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520357588104722e-5
allele num: 65774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.705043e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.93e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.717e1

QD
type: SiteQuality
SIO_000300: 1.836e1

MQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+697C>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+697C>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+697C>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+697C>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1320
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7470
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7352
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1287
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3063
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1989
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 782
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 399
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6033
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6706
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6212
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4540
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6975
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4324
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1980
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27572
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3499
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10962
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.208866261020738e-5
allele num: 16106
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.917e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.543e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.273e0

QD
type: SiteQuality
SIO_000300: 1.085e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.139e0

DP
type: SiteQuality
SIO_000300: 2.69606e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429469
ensembl transcript: ENST00000522874
gene symbol: MOK
hgvsc: ENST00000522874.1:c.864-23C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+691C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453224
ensembl transcript: ENST00000517966
gene symbol: MOK
hgvsc: ENST00000517966.1:c.64+691C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.374-23C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 6212
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1990
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 851
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6936
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7462
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4539
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1720
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7351
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5707
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 287
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2720
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 827
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6578
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1286
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 399
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3591
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 469
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4202
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3873
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10196
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3474
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27571
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1880
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52522725886157e-5
allele num: 65564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10028
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16066
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.411e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.392e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 2.685271e6

QD
type: SiteQuality
SIO_000300: 1.415e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1838C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000355304
ensembl transcript: ENST00000361847
gene symbol: MOK
hgvsc: ENST00000361847.2:c.867-29C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+685C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+685C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 6866
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 322
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5292
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2164
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2366
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7445
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1468
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1989
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6307
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7349
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4538
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6212
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1286
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1840
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3870
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3444
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9190
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4051
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27564
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16042
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527230520174715e-5
allele num: 65478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.286e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

QD
type: SiteQuality
SIO_000300: 1.371e1

VQSLOD
type: SiteQuality
SIO_000300: -6.133999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.132e0

MQRankSum
type: SiteQuality
SIO_000300: -1.316e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 2.670091e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519569
gene symbol: MOK
hgvsc: ENST00000519569.1:n.1509-29C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+685C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+685C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453224
ensembl transcript: ENST00000517966
gene symbol: MOK
hgvsc: ENST00000517966.1:c.64+685C>G
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2366
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7349
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1286
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1989
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6307
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2164
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7445
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1468
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5292
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6866
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4538
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6212
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3444
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9190
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4051
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1840
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27564
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3870
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.738203425375742e-5
allele num: 11444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65478
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.85e-1

FS
type: SiteQuality
SIO_000300: 6.286e0

MQRankSum
type: SiteQuality
SIO_000300: -1.316e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.132e0

DP
type: SiteQuality
SIO_000300: 2.670091e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.133999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.371e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+670G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+670G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000518686
gene symbol: MOK
hgvsc: ENST00000518686.1:n.2054-44G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+670G>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 398
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2442
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2516
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4535
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7338
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5235
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6618
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1989
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3668
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1068
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7395
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 377
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6212
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3783
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1286
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3286
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6392
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27543
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 233
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1463
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3850
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3324
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9962
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.071064430931761e-5
allele num: 65124
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: 2
allele frequency: 1.264382349222405e-4
allele num: 15818
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.484e0

MQRankSum
type: SiteQuality
SIO_000300: 4.02e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 1.2504e1

QD
type: SiteQuality
SIO_000300: 1.462e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 2.628731e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453224
ensembl transcript: ENST00000517966
gene symbol: MOK
hgvsc: ENST00000517966.1:c.64+669C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+669C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453762
ensembl transcript: ENST00000523231
gene symbol: MOK
hgvsc: ENST00000523231.1:c.64+669C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+669C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 2773
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1286
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4533
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7332
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5129
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1989
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2450
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3671
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6210
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1089
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 376
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3652
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6586
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7386
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3842
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6186
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27534
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2352
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1529
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9938
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.536570374923171e-5
allele num: 65080
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15806
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.303e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.17e0

DP
type: SiteQuality
SIO_000300: 2.625756e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.271e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.374-50C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000518686
gene symbol: MOK
hgvsc: ENST00000518686.1:n.2054-50C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+664C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000193029
ensembl transcript: ENST00000193029
gene symbol: MOK
hgvsc: ENST00000193029.6:c.164+664C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 376
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3533
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1990
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1180
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6480
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7357
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2432
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 398
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3499
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1285
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6209
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7328
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3590
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4665
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4533
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3517
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2057
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1830
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2985
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4142
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1883
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27536
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1505
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1612
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3835
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15742
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.766444232602478e-4
allele num: 8392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9888
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.617e0

QD
type: SiteQuality
SIO_000300: 1.185e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.617116e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.87e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+663G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+663G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+663G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+663G>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 4533
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3559
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7354
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4617
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6458
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1189
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1285
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3107
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3584
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2428
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6209
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7327
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1990
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3548
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2936
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1872
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3835
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1839
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27532
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1332
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3517
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1095
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542495758136665e-5
allele num: 64830
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15646
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.616484e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.852e0

QD
type: SiteQuality
SIO_000300: 1.159e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+47A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+47A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1200A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520252
gene symbol: MOK
hgvsc: ENST00000520252.1:n.444+47A>G
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 187
bin: 8.75e1
variant carriers: 30

GenotypeDepth
all individuals: 2217
bin: 7.5e0
variant carriers: 8

GenotypeDepth
all individuals: 672
bin: 9.75e1
variant carriers: 103

GenotypeDepth
all individuals: 498
bin: 6.25e1
variant carriers: 16

GenotypeDepth
all individuals: 359
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2068
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 672
bin: 1.75e1
variant carriers: 6

GenotypeDepth
all individuals: 4905
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 924
bin: 5.25e1
variant carriers: 8

GenotypeDepth
all individuals: 22726
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1246
bin: 4.75e1
variant carriers: 5

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 35

GenotypeDepth
all individuals: 152
bin: 9.25e1
variant carriers: 27

GenotypeDepth
all individuals: 4149
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2150
bin: 1.25e1
variant carriers: 8

GenotypeDepth
all individuals: 231
bin: 7.75e1
variant carriers: 28

GenotypeDepth
all individuals: 270
bin: 7.25e1
variant carriers: 17

GenotypeDepth
all individuals: 380
bin: 6.75e1
variant carriers: 20

GenotypeDepth
all individuals: 601
bin: 5.75e1
variant carriers: 11

GenotypeDepth
all individuals: 16037
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1809
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2606
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 529
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 185
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 243
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6008
bin: 9.75e1
variant carriers: 318

GenotypeQuality
all individuals: 3133
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 8.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 213
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30050
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2127
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 9285
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 249
allele frequency: 3.813637199044293e-3
allele num: 65292
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.480278422273782e-3
allele num: 862
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 1.64758931668401e-3
allele num: 11532
num of homozygotes: 0

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

South Asian
type: Population
allele count: 40
allele frequency: 3.093102381688834e-3
allele num: 12932
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.883495145631068e-4
allele num: 10300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

QD
type: SiteQuality
SIO_000300: 1.434e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.35e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 1.905522e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520252
gene symbol: MOK
hgvsc: ENST00000520252.1:n.444+46A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+46A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000518686
gene symbol: MOK
hgvsc: ENST00000518686.1:n.2053+46A>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+46A>G
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 128
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 572
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 224
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 662
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2215
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16137
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2079
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22837
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2156
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 596
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4934
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4175
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1252
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 361
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 921
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5723
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 381
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9330
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1850
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1222
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12930
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.063068582105553e-5
allele num: 65294
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.472e0

MQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

FS
type: SiteQuality
SIO_000300: 5.08e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.48e0

VQSLOD
type: SiteQuality
SIO_000300: 6.72e-1

DP
type: SiteQuality
SIO_000300: 1.888552e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

QD
type: SiteQuality
SIO_000300: 1.399e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1196G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+43G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453401
ensembl transcript: ENST00000559138
gene symbol: MOK
hgvsc: ENST00000559138.1:c.64+43G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453799
ensembl transcript: ENST00000522537
gene symbol: MOK
hgvsc: ENST00000522537.1:c.64+43G>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 2079
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22837
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 654
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 596
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1252
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2179
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4212
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4933
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2180
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 921
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16143
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 361
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 571
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1901
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9330
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30267
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1222
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 517
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5719
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 861
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2612
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3147
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12864
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.316423442205235e-4
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65284
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.922e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.577e0

VQSLOD
type: SiteQuality
SIO_000300: 4.78e-1

FS
type: SiteQuality
SIO_000300: 2.611e0

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-1

DP
type: SiteQuality
SIO_000300: 1.88932e6

QD
type: SiteQuality
SIO_000300: 1.184e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+40C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1193C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519569
gene symbol: MOK
hgvsc: ENST00000519569.1:n.1508+40C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+40C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 2181
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2161
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 596
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4315
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22850
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 361
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2077
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16142
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1253
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 921
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4934
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2069
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30397
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2611
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9340
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3149
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5718
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13046
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65338
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.35e-1

DP
type: SiteQuality
SIO_000300: 1.890494e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.813e0

QD
type: SiteQuality
SIO_000300: 1.456e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453224
ensembl transcript: ENST00000517966
gene symbol: MOK
hgvsc: ENST00000517966.1:c.64+35A>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+35A>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1188A>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000557823
gene symbol: MOK
hgvsc: ENST00000557823.1:n.172+1188A>C
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4932
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16144
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 220
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 550
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2077
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2106
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2154
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4494
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 362
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 22877
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 595
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 921
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1254
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30575
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2198
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5718
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 147
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9353
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.059601028025946e-5
allele num: 65368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13136
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.525e0

MQ
type: SiteQuality
SIO_000300: 5.853e1

VQSLOD
type: SiteQuality
SIO_000300: -1.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-2

QD
type: SiteQuality
SIO_000300: 1.04e1

DP
type: SiteQuality
SIO_000300: 1.89311e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+34C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454098
ensembl transcript: ENST00000522867
gene symbol: MOK
hgvsc: ENST00000522867.1:c.64+34C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429672
ensembl transcript: ENST00000519058
gene symbol: MOK
hgvsc: ENST00000519058.1:c.64+34C>G
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000355304
ensembl transcript: ENST00000361847
gene symbol: MOK
hgvsc: ENST00000361847.2:c.866+34C>G
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 4932
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22884
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 127
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2159
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 595
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4555
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 198
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2077
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 921
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16149
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2078
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1254
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 523
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 361
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2216
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30626
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9359
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 848
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5718
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65368
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.516760200212346e-4
allele num: 13186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.42e0

QD
type: SiteQuality
SIO_000300: 1.651e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.738e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 6.012e0

DP
type: SiteQuality
SIO_000300: 1.893896e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000518686
gene symbol: MOK
hgvsc: ENST00000518686.1:n.2053+29A>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+29A>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429348
ensembl transcript: ENST00000521766
gene symbol: MOK
hgvsc: ENST00000521766.1:c.*1504+29A>C
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000519477
gene symbol: MOK
hgvsc: ENST00000519477.1:n.373+29A>C
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 4868
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 595
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4932
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16150
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22935
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1254
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2077
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2088
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 361
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1916
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 921
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9380
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2229
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3157
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2615
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30936
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2137
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5716
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 759
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.459346561241235e-5
allele num: 13406
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65444
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.104e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 1.898323e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 6.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.196e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.087e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+28C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453950
ensembl transcript: ENST00000561150
gene symbol: MOK
hgvsc: ENST00000561150.1:c.64+28C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000193029
ensembl transcript: ENST00000193029
gene symbol: MOK
hgvsc: ENST00000193029.6:c.164+28C>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+28C>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 4932
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 595
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2056
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 4968
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1254
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 361
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2077
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16152
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1876
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 921
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 568
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 22948
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2137
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5716
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 406
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9382
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31022
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3155
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2619
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13422
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65446
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.691800736576855e-5
allele num: 10318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.98e1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 5.661e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 1.899411e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.178e0

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.501e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+24G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000518686
gene symbol: MOK
hgvsc: ENST00000518686.1:n.2053+24G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+24G>T
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000429469
ensembl transcript: ENST00000522874
gene symbol: MOK
hgvsc: ENST00000522874.1:c.863+24G>T
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 16157
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 920
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1699
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5194
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 361
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 594
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4932
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23034
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1889
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2077
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1254
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5720
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9404
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2623
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31231
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2067
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3156
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525041176111755e-5
allele num: 65572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

FS
type: SiteQuality
SIO_000300: 9.364000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.48e-1

DP
type: SiteQuality
SIO_000300: 1.904592e6

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

QD
type: SiteQuality
SIO_000300: 1.198e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000454203
ensembl transcript: ENST00000522534
gene symbol: MOK
hgvsc: ENST00000522534.1:c.64+24G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000452978
ensembl transcript: ENST00000524370
gene symbol: MOK
hgvsc: ENST00000524370.1:c.64+24G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl protein: ENSP00000453224
ensembl transcript: ENST00000517966
gene symbol: MOK
hgvsc: ENST00000517966.1:c.64+24G>A
variant of: http://identifiers.org/hgnc/9833

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000080823
ensembl transcript: ENST00000520266
gene symbol: MOK
hgvsc: ENST00000520266.1:n.293+1177G>A
variant of: http://identifiers.org/hgnc/9833

GenotypeDepth
all individuals: 159
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 569
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1699
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5194
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 23034
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 361
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16157
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2077
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 127
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1254
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 594
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 920
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4932
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1889
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9404
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 8.25e1
variant carriers: 0