16-29842273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842273
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842273
    reference: chr 16
allele count: 18
allele frequency: 1.486743206409515e-4
allele num: 121070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+316G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+278G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+278G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000563096
  gene symbol: MVP
  hgvsc: ENST00000563096.1:n.524G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+278G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.200G>A
  hgvsp: ENSP00000454825.1:p.Arg67Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.200G>A
  hgvsp: ENSP00000378760.1:p.Arg67Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.200G>A
  hgvsp: ENSP00000456291.1:p.Arg67Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.200G>A
  hgvsp: ENSP00000455819.1:p.Arg67Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.200G>A
  hgvsp: ENSP00000457685.1:p.Arg67Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.200G>A
  hgvsp: ENSP00000349977.5:p.Arg67Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.200G>A
  hgvsp: ENSP00000455186.1:p.Arg67Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.310G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Arg67Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

16-29842279-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842279
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842279
    reference: chr 16
allele count: 2
allele frequency: 1.651718613217052e-5
allele num: 121086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.206C>G
  hgvsp: ENSP00000456291.1:p.Ala69Gly
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.206C>G
  hgvsp: ENSP00000349977.5:p.Ala69Gly
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.206C>G
  hgvsp: ENSP00000378760.1:p.Ala69Gly
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+284C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.206C>G
  hgvsp: ENSP00000454825.1:p.Ala69Gly
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.206C>G
  hgvsp: ENSP00000455819.1:p.Ala69Gly
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.316C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000563096
  gene symbol: MVP
  hgvsc: ENST00000563096.1:n.530C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.206C>G
  hgvsp: ENSP00000455186.1:p.Ala69Gly
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+322C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+284C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+284C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.206C>G
  hgvsp: ENSP00000457685.1:p.Ala69Gly
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala69Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

16-29842285-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842285
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842285
    reference: chr 16
allele count: 1
allele frequency: 8.259957378619926e-6
allele num: 121066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.212G>A
  hgvsp: ENSP00000455186.1:p.Gly71Asp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.212G>A
  hgvsp: ENSP00000454825.1:p.Gly71Asp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+290G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.322G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.212G>A
  hgvsp: ENSP00000457685.1:p.Gly71Asp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.212G>A
  hgvsp: ENSP00000378760.1:p.Gly71Asp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.212G>A
  hgvsp: ENSP00000456291.1:p.Gly71Asp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.212G>A
  hgvsp: ENSP00000349977.5:p.Gly71Asp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+328G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+290G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000563096
  gene symbol: MVP
  hgvsc: ENST00000563096.1:n.536G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.212G>A
  hgvsp: ENSP00000455819.1:p.Gly71Asp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+290G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly71Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

16-29842298-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842298
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842298
    reference: chr 16
allele count: 2
allele frequency: 1.652373634726284e-5
allele num: 121038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.225T>A
  hgvsp: ENSP00000455186.1:p.Phe75Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.225T>A
  hgvsp: ENSP00000378760.1:p.Phe75Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.335T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+303T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+341T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.225T>A
  hgvsp: ENSP00000455819.1:p.Phe75Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+303T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.225T>A
  hgvsp: ENSP00000349977.5:p.Phe75Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.225T>A
  hgvsp: ENSP00000454825.1:p.Phe75Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.225T>A
  hgvsp: ENSP00000457685.1:p.Phe75Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+303T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.225T>A
  hgvsp: ENSP00000456291.1:p.Phe75Leu
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe75Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

16-29842299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842299
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842299
    reference: chr 16
allele count: 1
allele frequency: 8.262687356435807e-6
allele num: 121026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+342G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.336G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.226G>A
  hgvsp: ENSP00000457685.1:p.Asp76Asn
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.226G>A
  hgvsp: ENSP00000349977.5:p.Asp76Asn
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.226G>A
  hgvsp: ENSP00000454825.1:p.Asp76Asn
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+304G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.226G>A
  hgvsp: ENSP00000455819.1:p.Asp76Asn
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.226G>A
  hgvsp: ENSP00000455186.1:p.Asp76Asn
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.226G>A
  hgvsp: ENSP00000378760.1:p.Asp76Asn
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.226G>A
  hgvsp: ENSP00000456291.1:p.Asp76Asn
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+304G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+304G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp76Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

16-29842303-T-TCACA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842303
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842307
    reference: chr 16
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: TCACA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.341_344dupCACA
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.231_234dupCACA
  hgvsp: ENSP00000454825.1:p.Gly79HisfsTer10
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+309_125+312dupCACA
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.231_234dupCACA
  hgvsp: ENSP00000455819.1:p.Gly79HisfsTer10
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+309_125+312dupCACA
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.231_234dupCACA
  hgvsp: ENSP00000349977.5:p.Gly79HisfsTer10
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+309_76+312dupCACA
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.231_234dupCACA
  hgvsp: ENSP00000455186.1:p.Gly79HisfsTer10
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+347_87+350dupCACA
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.231_234dupCACA
  hgvsp: ENSP00000456291.1:p.Gly79HisfsTer10
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.231_234dupCACA
  hgvsp: ENSP00000457685.1:p.Gly79HisfsTer10
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.231_234dupCACA
  hgvsp: ENSP00000378760.1:p.Gly79HisfsTer10
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly79HisfsTer10
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ

16-29842306-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842306
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842304
    reference: chr 16
allele count: 4
allele frequency: 3.306932985003059e-5
allele num: 120958
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.234_235delAG
  hgvsp: ENSP00000455819.1:p.Gly79AlafsTer8
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.234_235delAG
  hgvsp: ENSP00000457685.1:p.Gly79AlafsTer8
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.234_235delAG
  hgvsp: ENSP00000456291.1:p.Gly79AlafsTer8
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.344_345delAG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.234_235delAG
  hgvsp: ENSP00000455186.1:p.Gly79AlafsTer8
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.234_235delAG
  hgvsp: ENSP00000349977.5:p.Gly79AlafsTer8
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.234_235delAG
  hgvsp: ENSP00000454825.1:p.Gly79AlafsTer8
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+350_87+351delAG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+312_125+313delAG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+312_76+313delAG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.234_235delAG
  hgvsp: ENSP00000378760.1:p.Gly79AlafsTer8
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+312_125+313delAG
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly79AlafsTer8
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: CAG
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

16-29842307-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842307
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842307
    reference: chr 16
allele count: 4
allele frequency: 3.307097030226867e-5
allele num: 120952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.234A>G
  hgvsp: ENST00000563915.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.234A>G
  hgvsp: ENST00000563558.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+350A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.234A>G
  hgvsp: ENST00000570234.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.234A>G
  hgvsp: ENST00000357402.5:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+312A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.234A>G
  hgvsp: ENST00000566066.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.234A>G
  hgvsp: ENST00000566252.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+312A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.234A>G
  hgvsp: ENST00000395353.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.344A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+312A>G
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr78Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

16-29842318-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842318
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842318
    reference: chr 16
allele count: 4
allele frequency: 3.308355251186872e-5
allele num: 120906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.245G>A
  hgvsp: ENSP00000456291.1:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.245G>A
  hgvsp: ENSP00000454825.1:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.245G>A
  hgvsp: ENSP00000349977.5:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.245G>A
  hgvsp: ENSP00000457685.1:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+323G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.245G>A
  hgvsp: ENSP00000455186.1:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+323G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.245G>A
  hgvsp: ENSP00000378760.1:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+361G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.245G>A
  hgvsp: ENSP00000455819.1:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+323G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.355G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg82Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

16-29842319-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842319
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842319
    reference: chr 16
allele count: 1
allele frequency: 8.272119647938589e-6
allele num: 120888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.246G>T
  hgvsp: ENST00000570234.1:c.246G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+324G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.246G>T
  hgvsp: ENST00000566252.1:c.246G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.246G>T
  hgvsp: ENST00000357402.5:c.246G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.246G>T
  hgvsp: ENST00000563558.1:c.246G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+324G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+362G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.246G>T
  hgvsp: ENST00000566066.1:c.246G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.246G>T
  hgvsp: ENST00000395353.1:c.246G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.246G>T
  hgvsp: ENST00000563915.1:c.246G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.356G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+324G>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg82Arg
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

16-29842323-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842323
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842323
    reference: chr 16
allele count: 22
allele frequency: 1.820077105084634e-4
allele num: 120874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+328C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.360C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.250C>T
  hgvsp: ENSP00000378760.1:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.250C>T
  hgvsp: ENSP00000456291.1:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.250C>T
  hgvsp: ENSP00000349977.5:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.250C>T
  hgvsp: ENSP00000457685.1:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+328C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.250C>T
  hgvsp: ENSP00000454825.1:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.250C>T
  hgvsp: ENSP00000455186.1:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.250C>T
  hgvsp: ENSP00000455819.1:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+328C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+366C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg84Cys
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

16-29842324-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842324
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842324
    reference: chr 16
allele count: 14
allele frequency: 1.15836505047162e-4
allele num: 120860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+329G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.251G>A
  hgvsp: ENSP00000349977.5:p.Arg84His
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+329G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.251G>A
  hgvsp: ENSP00000454825.1:p.Arg84His
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.361G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.251G>A
  hgvsp: ENSP00000455186.1:p.Arg84His
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+329G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.251G>A
  hgvsp: ENSP00000457685.1:p.Arg84His
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.251G>A
  hgvsp: ENSP00000455819.1:p.Arg84His
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.251G>A
  hgvsp: ENSP00000456291.1:p.Arg84His
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.251G>A
  hgvsp: ENSP00000378760.1:p.Arg84His
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+367G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg84His
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS

16-29842329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842329
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842329
    reference: chr 16
allele count: 1
allele frequency: 8.278831029058698e-6
allele num: 120790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.256G>A
  hgvsp: ENSP00000454825.1:p.Ala86Thr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.256G>A
  hgvsp: ENSP00000456291.1:p.Ala86Thr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.256G>A
  hgvsp: ENSP00000455186.1:p.Ala86Thr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.256G>A
  hgvsp: ENSP00000349977.5:p.Ala86Thr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+334G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+372G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.256G>A
  hgvsp: ENSP00000455819.1:p.Ala86Thr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+334G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.366G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.256G>A
  hgvsp: ENSP00000378760.1:p.Ala86Thr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.256G>A
  hgvsp: ENSP00000457685.1:p.Ala86Thr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+334G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala86Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD

16-29842329-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842329
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842329
    reference: chr 16
allele count: 1
allele frequency: 8.278831029058698e-6
allele num: 120790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.256G>T
  hgvsp: ENSP00000455819.1:p.Ala86Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.256G>T
  hgvsp: ENSP00000454825.1:p.Ala86Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+372G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.256G>T
  hgvsp: ENSP00000378760.1:p.Ala86Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+334G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+334G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+334G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.256G>T
  hgvsp: ENSP00000349977.5:p.Ala86Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.256G>T
  hgvsp: ENSP00000455186.1:p.Ala86Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.366G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.256G>T
  hgvsp: ENSP00000457685.1:p.Ala86Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.256G>T
  hgvsp: ENSP00000456291.1:p.Ala86Ser
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala86Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-29842338-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842338
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842338
    reference: chr 16
allele count: 1
allele frequency: 8.290911502810618e-6
allele num: 120614
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+343G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.265G>A
  hgvsp: ENSP00000455819.1:p.Glu89Lys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.265G>A
  hgvsp: ENSP00000457685.1:p.Glu89Lys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.265G>A
  hgvsp: ENSP00000349977.5:p.Glu89Lys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+381G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.375G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.265G>A
  hgvsp: ENSP00000456291.1:p.Glu89Lys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.265G>A
  hgvsp: ENSP00000454825.1:p.Glu89Lys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+343G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.265G>A
  hgvsp: ENSP00000378760.1:p.Glu89Lys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.265G>A
  hgvsp: ENSP00000455186.1:p.Glu89Lys
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+343G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu89Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

16-29842338-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842338
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842338
    reference: chr 16
allele count: 1
allele frequency: 8.290911502810618e-6
allele num: 120614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.265G>C
  hgvsp: ENSP00000454825.1:p.Glu89Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.265G>C
  hgvsp: ENSP00000456291.1:p.Glu89Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+343G>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.265G>C
  hgvsp: ENSP00000455819.1:p.Glu89Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+381G>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.265G>C
  hgvsp: ENSP00000455186.1:p.Glu89Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+343G>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.265G>C
  hgvsp: ENSP00000378760.1:p.Glu89Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.265G>C
  hgvsp: ENSP00000457685.1:p.Glu89Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+343G>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.375G>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.265G>C
  hgvsp: ENSP00000349977.5:p.Glu89Gln
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu89Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

16-29842344-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842344
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842344
    reference: chr 16
allele count: 2
allele frequency: 1.660026560424967e-5
allele num: 120480
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.271C>T
  hgvsp: ENSP00000349977.5:p.Arg91Trp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.271C>T
  hgvsp: ENSP00000457685.1:p.Arg91Trp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+349C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.271C>T
  hgvsp: ENSP00000378760.1:p.Arg91Trp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+349C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.381C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+387C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.271C>T
  hgvsp: ENSP00000455186.1:p.Arg91Trp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.271C>T
  hgvsp: ENSP00000455819.1:p.Arg91Trp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.271C>T
  hgvsp: ENSP00000456291.1:p.Arg91Trp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.271C>T
  hgvsp: ENSP00000454825.1:p.Arg91Trp
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+349C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3834
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg91Trp
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

16-29842345-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842345
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842345
    reference: chr 16
allele count: 3
allele frequency: 2.491404653943893e-5
allele num: 120414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+350G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.272G>A
  hgvsp: ENSP00000455819.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.272G>A
  hgvsp: ENSP00000455186.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+350G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+350G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.272G>A
  hgvsp: ENSP00000349977.5:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.382G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.272G>A
  hgvsp: ENSP00000454825.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+388G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.272G>A
  hgvsp: ENSP00000457685.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.272G>A
  hgvsp: ENSP00000378760.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.272G>A
  hgvsp: ENSP00000456291.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33904
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg91Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

16-29842346-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842346
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842346
    reference: chr 16
allele count: 2
allele frequency: 1.66096402351925e-5
allele num: 120412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.273G>A
  hgvsp: ENST00000395353.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+389G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455186
  ensembl transcript: ENST00000566066
  gene symbol: MVP
  hgvsc: ENST00000566066.1:c.273G>A
  hgvsp: ENST00000566066.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.273G>A
  hgvsp: ENST00000563558.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.273G>A
  hgvsp: ENST00000566252.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.273G>A
  hgvsp: ENST00000357402.5:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+351G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.383G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.273G>A
  hgvsp: ENST00000570234.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.273G>A
  hgvsp: ENST00000563915.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+351G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+351G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg91Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

16-29842358-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842358
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842359
    reference: chr 16
allele count: 1
allele frequency: 8.336807002917883e-6
allele num: 119950
alternate allele: CT
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.285_286insT
  hgvsp: ENSP00000349977.5:p.Pro96SerfsTer33
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.285_286insT
  hgvsp: ENSP00000456291.1:p.Pro96SerfsTer33
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+363_76+364insT
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.395_396insT
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.285_286insT
  hgvsp: ENSP00000457685.1:p.Pro96SerfsTer?
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+401_87+402insT
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+363_125+364insT
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.285_286insT
  hgvsp: ENSP00000454825.1:p.Pro96SerfsTer?
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.285_286insT
  hgvsp: ENSP00000455819.1:p.Pro96SerfsTer33
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+363_125+364insT
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.285_286insT
  hgvsp: ENSP00000378760.1:p.Pro96SerfsTer33
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro96SerfsTer33
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

16-29842365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842365
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842365
    reference: chr 16
allele count: 1
allele frequency: 8.356033892073466e-6
allele num: 119674
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.292C>T
  hgvsp: ENSP00000454825.1:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.292C>T
  hgvsp: ENSP00000457685.1:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.292C>T
  hgvsp: ENSP00000378760.1:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+408C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.292C>T
  hgvsp: ENSP00000455819.1:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.402C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+370C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+370C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.292C>T
  hgvsp: ENSP00000456291.1:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.292C>T
  hgvsp: ENSP00000349977.5:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+370C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro98Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

16-29842366-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842366
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842366
    reference: chr 16
allele count: 1
allele frequency: 8.356313194618534e-6
allele num: 119670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.403C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.293C>T
  hgvsp: ENSP00000457685.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+409C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.293C>T
  hgvsp: ENSP00000349977.5:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.293C>T
  hgvsp: ENSP00000378760.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+371C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+371C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.293C>T
  hgvsp: ENSP00000454825.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.293C>T
  hgvsp: ENSP00000456291.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.293C>T
  hgvsp: ENSP00000455819.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+371C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro98Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-29842375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842375
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842375
    reference: chr 16
allele count: 1
allele frequency: 8.401102224611869e-6
allele num: 119032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.302C>T
  hgvsp: ENSP00000455819.1:p.Pro101Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.412C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.302C>T
  hgvsp: ENSP00000454825.1:p.Pro101Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+380C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.302C>T
  hgvsp: ENSP00000349977.5:p.Pro101Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+418C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+380C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.302C>T
  hgvsp: ENSP00000456291.1:p.Pro101Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.302C>T
  hgvsp: ENSP00000457685.1:p.Pro101Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.302C>T
  hgvsp: ENSP00000378760.1:p.Pro101Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+380C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro101Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

16-29842380-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842380
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842380
    reference: chr 16
allele count: 1
allele frequency: 8.442808415791428e-6
allele num: 118444
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.307G>C
  hgvsp: ENSP00000378760.1:p.Glu103Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+385G>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+423G>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+385G>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.307G>C
  hgvsp: ENSP00000454825.1:p.Glu103Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.307G>C
  hgvsp: ENSP00000349977.5:p.Glu103Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+385G>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.307G>C
  hgvsp: ENSP00000455819.1:p.Glu103Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.307G>C
  hgvsp: ENSP00000457685.1:p.Glu103Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.307G>C
  hgvsp: ENSP00000456291.1:p.Glu103Gln
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.417G>C
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu103Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

16-29842382-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842382
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842382
    reference: chr 16
allele count: 4
allele frequency: 3.379919895898467e-5
allele num: 118346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+387G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.309G>A
  hgvsp: ENST00000395353.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+425G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.309G>A
  hgvsp: ENST00000566252.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.309G>A
  hgvsp: ENST00000563915.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.309G>A
  hgvsp: ENST00000563558.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.419G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+387G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.309G>A
  hgvsp: ENST00000570234.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+387G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.309G>A
  hgvsp: ENST00000357402.5:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18279
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu103Glu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

16-29842390-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842390
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842390
    reference: chr 16
allele count: 1
allele frequency: 8.524277141298417e-6
allele num: 117312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.317A>T
  hgvsp: ENSP00000456291.1:p.Glu106Val
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+395A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+395A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.317A>T
  hgvsp: ENSP00000454825.1:p.Glu106Val
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.427A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.317A>T
  hgvsp: ENSP00000455819.1:p.Glu106Val
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+433A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457685
  ensembl transcript: ENST00000566252
  gene symbol: MVP
  hgvsc: ENST00000566252.1:c.317A>T
  hgvsp: ENSP00000457685.1:p.Glu106Val
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.317A>T
  hgvsp: ENSP00000378760.1:p.Glu106Val
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.317A>T
  hgvsp: ENSP00000349977.5:p.Glu106Val
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+395A>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu106Val
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

16-29842399-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842399
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842399
    reference: chr 16
allele count: 5
allele frequency: 4.320027648176949e-5
allele num: 115740
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+5C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+5C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+5C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.431+5C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+404C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+5C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+442C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+404C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+5C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+404C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16288
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7038
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 3.25e1
  variant carriers: 0
hgvs: c.321+5C>T
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

16-29842401-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842401
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842401
    reference: chr 16
allele count: 10
allele frequency: 8.654861435668415e-5
allele num: 115542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+406G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+7G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+7G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+7G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.431+7G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+7G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+444G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+406G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+406G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+7G>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16072
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26941
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
hgvs: c.321+7G>T
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

16-29842405-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842405
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842405
    reference: chr 16
allele count: 7
allele frequency: 6.093526933389045e-5
allele num: 114876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+448T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.431+11T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+410T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+410T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+11T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+410T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+11T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+11T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+11T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+11T>C
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25315
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8977
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14985
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2971
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

16-29842407-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842407
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842407
    reference: chr 16
allele count: 1
allele frequency: 8.738814317673378e-6
allele num: 114432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+450C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+412C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+13C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+412C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+13C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+13C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+412C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+13C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+13C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.431+13C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9914
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3382
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

16-29842409-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842409
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842409
    reference: chr 16
allele count: 10
allele frequency: 8.771622048349181e-5
allele num: 114004
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+15C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+452C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+414C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+414C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.431+15C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+15C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+15C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+414C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+15C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+15C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13600
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 22889
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30507
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3395
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

16-29842414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842414
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842414
    reference: chr 16
allele count: 2
allele frequency: 1.767596422384841e-5
allele num: 113148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+20C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+419C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+419C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+457C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.431+20C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+419C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+20C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+20C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+20C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+20C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12730
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20808
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3969
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

16-29842417-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842417
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842417
    reference: chr 16
allele count: 1
allele frequency: 8.876895217128857e-6
allele num: 112652
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+460A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+422A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+23A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+422A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+23A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.431+23A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+23A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+23A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+23A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+422A>G
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11483
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5317
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS

16-29842425-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842425
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842425
    reference: chr 16
allele count: 1
allele frequency: 9.025759517663412e-6
allele num: 110794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+430C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+31C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+468C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.431+31C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+31C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+430C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+31C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+31C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+31C>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+430C>G
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15658
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8776
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

16-29842437-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842437
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842437
    reference: chr 16
allele count: 1
allele frequency: 9.287638153617536e-6
allele num: 107670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+43T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+442T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+442T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.431+43T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+43T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+442T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+43T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+480T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+43T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+43T>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17325
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2471
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

16-29842939-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29842939
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29842939
    reference: chr 16
allele count: 1
allele frequency: 9.235315847801995e-5
allele num: 10828
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+545A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+545A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+545A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+982A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+944A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+545A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+944A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.432-26A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+944A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+545A>G
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS

16-29843002-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29843002
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29843002
    reference: chr 16
allele count: 1
allele frequency: 9.271277582050807e-5
allele num: 10786
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+1007A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+1007A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+608A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+608A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+1007A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+608A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+608A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+1045A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.469A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+608A>G
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

16-29843041-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29843041
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29843041
    reference: chr 16
allele count: 2
allele frequency: 1.854943424225561e-4
allele num: 10782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+647C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.508C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+1046C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+1084C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+647C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+647C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+647C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+1046C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+1046C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+647C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

16-29843047-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29843047
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29843047
    reference: chr 16
allele count: 1
allele frequency: 9.267840593141798e-5
allele num: 10790
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.321+653C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.321+653C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.76+1052C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000565830
  gene symbol: MVP
  hgvsc: ENST00000565830.1:n.514C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.321+653C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.321+653C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.125+1052C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+653C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+1090C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.125+1052C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

16-29845005-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845005
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845004
    reference: chr 16
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.322-45delG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+3052delG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2072delG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2615delG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2072delG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.322-45delG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.352delG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.322-45delG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.322-45delG
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.126-45delG
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9675
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: TG
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ

16-29845008-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845008
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845008
    reference: chr 16
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.322-46G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.351G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.322-46G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.126-46G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2614G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2073G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.322-46G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+3051G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2073G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.322-46G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30758
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9653
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

16-29845011-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845011
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845011
    reference: chr 16
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+3054C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2617C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.322-43C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2070C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.354C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.322-43C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.322-43C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.126-43C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2070C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.322-43C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/16-29845016-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845016
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845016
    reference: chr 16
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.126-38C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2622C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2065C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.322-38C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.322-38C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+3059C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.322-38C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.322-38C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2065C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.359C>A
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2196
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

16-29845016-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845016
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845016
    reference: chr 16
allele count: 2
allele frequency: 1.650219479190732e-5
allele num: 121196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.87+3059C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.322-38C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2065C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2622C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.322-38C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.359C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2065C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.322-38C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.126-38C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.322-38C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9652
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

16-29845025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845025
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845025
    reference: chr 16
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.322-29T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.322-29T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2631T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2056T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.368T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2056T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.322-29T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3067T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.126-29T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.322-29T>C
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: T
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

16-29845028-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845028
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845028
    reference: chr 16
allele count: 2
allele frequency: 1.649076517150396e-5
allele num: 121280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2634T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2053T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3064T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.322-26T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.371T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.322-26T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2053T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.322-26T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.322-26T>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.126-26T>A
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

16-29845040-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845040
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845040
    reference: chr 16
allele count: 4
allele frequency: 3.296956908773203e-5
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2646T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.383T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3052T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.322-14T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2041T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.322-14T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.322-14T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.126-14T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2041T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.322-14T>C
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11798
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

16-29845048-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845048
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845048
    reference: chr 16
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2033C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2033C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2654C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.322-6C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.322-6C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.322-6C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.391C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.126-6C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.322-6C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3044C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11819
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: c.322-6C>T
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum

16-29845057-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845057
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845057
    reference: chr 16
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.129A>G
  hgvsp: ENST00000562463.1:c.129A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.325A>G
  hgvsp: ENSP00000455819.1:p.Ile109Val
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2663A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.325A>G
  hgvsp: ENSP00000456291.1:p.Ile109Val
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.400A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.325A>G
  hgvsp: ENSP00000378760.1:p.Ile109Val
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.325A>G
  hgvsp: ENSP00000349977.5:p.Ile109Val
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2024A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3035A>G
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2024A>G
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31683
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44204
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile109Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

16-29845064-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845064
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845064
    reference: chr 16
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3028C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.136C>T
  hgvsp: ENSP00000457734.1:p.Pro46Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.407C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.332C>T
  hgvsp: ENSP00000349977.5:p.Pro111Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.332C>T
  hgvsp: ENSP00000456291.1:p.Pro111Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2017C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.332C>T
  hgvsp: ENSP00000455819.1:p.Pro111Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2670C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.332C>T
  hgvsp: ENSP00000378760.1:p.Pro111Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2017C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11822
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31696
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro111Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/16-29845065-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845065
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845065
    reference: chr 16
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.408C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3027C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.137C>A
  hgvsp: ENSP00000457734.1:p.Pro46His
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.333C>A
  hgvsp: ENST00000563915.1:c.333C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.333C>A
  hgvsp: ENST00000570234.1:c.333C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2016C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2016C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2671C>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.333C>A
  hgvsp: ENST00000395353.1:c.333C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.333C>A
  hgvsp: ENST00000357402.5:c.333C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1904
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro46His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

16-29845074-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845074
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845074
    reference: chr 16
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.342G>T
  hgvsp: ENST00000563915.1:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2007G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.342G>T
  hgvsp: ENST00000357402.5:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.417G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.342G>T
  hgvsp: ENST00000570234.1:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2007G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.146G>T
  hgvsp: ENSP00000457734.1:p.Trp49Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2680G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3018G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.342G>T
  hgvsp: ENST00000395353.1:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Trp49Leu
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

16-29845080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845080
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845080
    reference: chr 16
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2001G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.348G>A
  hgvsp: ENST00000570234.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.348G>A
  hgvsp: ENST00000395353.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2686G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.423G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.152G>A
  hgvsp: ENSP00000457734.1:p.Cys51Tyr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2001G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3012G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.348G>A
  hgvsp: ENST00000357402.5:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.348G>A
  hgvsp: ENST00000563915.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31732
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys51Tyr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

16-29845081-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845081
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845081
    reference: chr 16
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.424C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.153C>T
  hgvsp: ENST00000562463.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.349C>T
  hgvsp: ENSP00000455819.1:p.Pro117Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-2000C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-2000C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.349C>T
  hgvsp: ENSP00000378760.1:p.Pro117Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.349C>T
  hgvsp: ENSP00000349977.5:p.Pro117Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.349C>T
  hgvsp: ENSP00000456291.1:p.Pro117Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3011C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2687C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro117Ser
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

16-29845083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845083
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845083
    reference: chr 16
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.351C>T
  hgvsp: ENST00000570234.1:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3009C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2689C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.155C>T
  hgvsp: ENSP00000457734.1:p.Pro52Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1998C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1998C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.351C>T
  hgvsp: ENST00000563915.1:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.426C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.351C>T
  hgvsp: ENST00000357402.5:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.351C>T
  hgvsp: ENST00000395353.1:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2210
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro52Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

16-29845086-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845086
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845086
    reference: chr 16
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.158C>T
  hgvsp: ENSP00000457734.1:p.Thr53Ile
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.354C>T
  hgvsp: ENST00000395353.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.354C>T
  hgvsp: ENST00000570234.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2692C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.354C>T
  hgvsp: ENST00000357402.5:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.429C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.354C>T
  hgvsp: ENST00000563915.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1995C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3006C>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1995C>T
  variant of: http://identifiers.org/hgnc/7531
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr53Ile
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP

16-29845087-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845087
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845087
    reference: chr 16
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1994A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2693A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.355A>T
  hgvsp: ENSP00000455819.1:p.Thr119Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.159A>T
  hgvsp: ENST00000562463.1:c.159A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1994A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.355A>T
  hgvsp: ENSP00000349977.5:p.Thr119Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.430A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.355A>T
  hgvsp: ENSP00000456291.1:p.Thr119Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.355A>T
  hgvsp: ENSP00000378760.1:p.Thr119Ser
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-3005A>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr119Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

16-29845097-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845097
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845097
    reference: chr 16
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.365A>T
  hgvsp: ENSP00000378760.1:p.His122Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.169A>T
  hgvsp: ENSP00000457734.1:p.Ile57Phe
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2703A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-2995A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.440A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1984A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.365A>T
  hgvsp: ENSP00000455819.1:p.His122Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.365A>T
  hgvsp: ENSP00000349977.5:p.His122Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.365A>T
  hgvsp: ENSP00000456291.1:p.His122Leu
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1984A>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His122Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

16-29845107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845107
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845107
    reference: chr 16
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.375G>A
  hgvsp: ENST00000563915.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.*5G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.375G>A
  hgvsp: ENST00000395353.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.450G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.375G>A
  hgvsp: ENST00000357402.5:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1974G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2713G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.375G>A
  hgvsp: ENST00000570234.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1974G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-2985G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala125Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

16-29845126-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845126
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845126
    reference: chr 16
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.394A>T
  hgvsp: ENSP00000455819.1:p.Lys132Ter
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-2966A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1955A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.394A>T
  hgvsp: ENSP00000456291.1:p.Lys132Ter
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1955A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.394A>T
  hgvsp: ENSP00000378760.1:p.Lys132Ter
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.469A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2732A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.*24A>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.394A>T
  hgvsp: ENSP00000349977.5:p.Lys132Ter
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys132Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-29845132-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845132
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845132
    reference: chr 16
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2738G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.400G>A
  hgvsp: ENSP00000349977.5:p.Gly134Arg
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.400G>A
  hgvsp: ENSP00000456291.1:p.Gly134Arg
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.475G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1949G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.*30G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.400G>A
  hgvsp: ENSP00000378760.1:p.Gly134Arg
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.400G>A
  hgvsp: ENSP00000455819.1:p.Gly134Arg
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1949G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-2960G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly134Arg
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS

http://identifiers.org/exac.variant/16-29845139-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845139
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845139
    reference: chr 16
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.482A>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1942A>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1942A>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.407A>C
  hgvsp: ENSP00000455819.1:p.Lys136Thr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.407A>C
  hgvsp: ENSP00000349977.5:p.Lys136Thr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.407A>C
  hgvsp: ENSP00000456291.1:p.Lys136Thr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.407A>C
  hgvsp: ENSP00000378760.1:p.Lys136Thr
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2745A>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.*37A>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-2953A>C
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys136Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

16-29845140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845140
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845140
    reference: chr 16
allele count: 7
allele frequency: 5.765872623636783e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2746G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.408G>A
  hgvsp: ENST00000563915.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.408G>A
  hgvsp: ENST00000570234.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.483G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.408G>A
  hgvsp: ENST00000395353.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.408G>A
  hgvsp: ENST00000357402.5:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1941G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-2952G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1941G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.*38G>A
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys136Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

16-29845144-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845144
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845144
    reference: chr 16
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-2948G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.412G>A
  hgvsp: ENSP00000378760.1:p.Val138Met
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2750G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.412G>A
  hgvsp: ENSP00000349977.5:p.Val138Met
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.412G>A
  hgvsp: ENSP00000455819.1:p.Val138Met
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1937G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.487G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1937G>A
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.412G>A
  hgvsp: ENSP00000456291.1:p.Val138Met
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1904
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val138Met
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

16-29845146-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845146
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845146
    reference: chr 16
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.414G>T
  hgvsp: ENST00000357402.5:c.414G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-2946G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.414G>T
  hgvsp: ENST00000563915.1:c.414G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.489G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.414G>T
  hgvsp: ENST00000570234.1:c.414G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.414G>T
  hgvsp: ENST00000395353.1:c.414G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1935G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2752G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1935G>T
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.*44G>T
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31769
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val138Val
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-29845154-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845154
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845154
    reference: chr 16
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.*52A>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.422A>C
  hgvsp: ENSP00000349977.5:p.Asp141Ala
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.422A>C
  hgvsp: ENSP00000455819.1:p.Asp141Ala
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1927A>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.497A>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1927A>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2760A>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.422A>C
  hgvsp: ENSP00000456291.1:p.Asp141Ala
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-2938A>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000458583
  ensembl transcript: ENST00000563123
  gene symbol: MVP
  hgvsc: ENST00000563123.1:c.7A>C
  hgvsp: ENSP00000458583.1:p.Asp3Ala
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.422A>C
  hgvsp: ENSP00000378760.1:p.Asp141Ala
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31770
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp141Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

16-29845155-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845155
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845155
    reference: chr 16
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2761T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.423T>C
  hgvsp: ENST00000357402.5:c.423T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.498T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.*53T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.423T>C
  hgvsp: ENST00000563915.1:c.423T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000458583
  ensembl transcript: ENST00000563123
  gene symbol: MVP
  hgvsc: ENST00000563123.1:c.8T>C
  hgvsp: ENST00000563123.1:c.8T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1926T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1926T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.423T>C
  hgvsp: ENST00000570234.1:c.423T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.423T>C
  hgvsp: ENST00000395353.1:c.423T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-2937T>C
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp141Asp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

16-29845159-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29845159
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 29845159
    reference: chr 16
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000457734
  ensembl transcript: ENST00000562463
  gene symbol: MVP
  hgvsc: ENST00000562463.1:c.*57T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000458583
  ensembl transcript: ENST00000563123
  gene symbol: MVP
  hgvsc: ENST00000563123.1:c.12T>C
  hgvsp: ENSP00000458583.1:p.Trp5Arg
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000378760
  ensembl transcript: ENST00000395353
  gene symbol: MVP
  hgvsc: ENST00000395353.1:c.427T>C
  hgvsp: ENSP00000378760.1:p.Trp143Arg
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013364
  ensembl transcript: ENST00000569612
  gene symbol: MVP
  hgvsc: ENST00000569612.1:n.502T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000387916
  ensembl transcript: ENST00000452209
  gene symbol: MVP
  hgvsc: ENST00000452209.2:c.77-1922T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000456291
  ensembl transcript: ENST00000570234
  gene symbol: MVP
  hgvsc: ENST00000570234.1:c.427T>C
  hgvsp: ENSP00000456291.1:p.Trp143Arg
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455741
  ensembl transcript: ENST00000566859
  gene symbol: MVP
  hgvsc: ENST00000566859.1:c.126-1922T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455819
  ensembl transcript: ENST00000563915
  gene symbol: MVP
  hgvsc: ENST00000563915.1:c.427T>C
  hgvsp: ENSP00000455819.1:p.Trp143Arg
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000455532
  ensembl transcript: ENST00000569887
  gene symbol: MVP
  hgvsc: ENST00000569887.1:c.88-2933T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000454825
  ensembl transcript: ENST00000563558
  gene symbol: MVP
  hgvsc: ENST00000563558.1:c.321+2765T>C
  variant of: http://identifiers.org/hgnc/7531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013364
  ensembl protein: ENSP00000349977
  ensembl transcript: ENST00000357402
  gene symbol: MVP
  hgvsc: ENST00000357402.5:c.427T>C
  hgvsp: ENSP00000349977.5:p.Trp143Arg
  variant of: http://identifiers.org/hgnc/7531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp143Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
reference allele: T

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

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 9
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3943
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6456
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1383
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 48157
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1651
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.552245976459284e-4
allele num: 66608
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 2.965e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 1.500781e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
all individuals: 258
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6476
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48341
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1379
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
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: 6486
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.925669170036588e-4
allele num: 10386
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.23e-1

DP
type: SiteQuality
SIO_000300: 1.500039e6

FS
type: SiteQuality
SIO_000300: 3.731e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.018e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.137e1

GenotypeDepth
all individuals: 26
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 911
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 706
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6451
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48220
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1647
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.499111e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

QD
type: SiteQuality
SIO_000300: 1.126e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.727e0

FS
type: SiteQuality
SIO_000300: 9.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 14
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48171
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 349
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6414
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 135
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 704
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1644
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003003003003003e-5
allele num: 66600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
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: 11550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

QD
type: SiteQuality
SIO_000300: 1.495e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.6e-1

DP
type: SiteQuality
SIO_000300: 1.497624e6

VQSLOD
type: SiteQuality
SIO_000300: -2.768e0

FS
type: SiteQuality
SIO_000300: 1.8759e1

MQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3887
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48025
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6405
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 365
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
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: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.497363e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.32e-1

FS
type: SiteQuality
SIO_000300: 5.257e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.011e0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.038e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

QD
type: SiteQuality
SIO_000300: 1.41e1

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

GenotypeDepth
all individuals: 166
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6420
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 802
bin: 9.75e1
variant carriers: 1

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: 8.97e-1

MQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: -3.2e-2

QD
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SIO_000300: 9.949999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.647e1

GenotypeDepth
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variant carriers: 2

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.008893161879582e-5
allele num: 66568
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

MQRankSum
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SIO_000300: 6.6e-1

QD
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MQ
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.626e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

DP
type: SiteQuality
SIO_000300: 1.496701e6

GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.00943481265587e-5
allele num: 66562
num of homozygotes: 0

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

South Asian
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e-1

DP
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SIO_000300: 1.496243e6

InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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MQ
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.61e-1

BaseQRankSum
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SIO_000300: -1.431e0

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.508972855983407e-5
allele num: 66534
num of homozygotes: 0

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

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

VQSLOD
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SIO_000300: 3.11e0

QD
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SIO_000300: 1.245e1

DP
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SIO_000300: 1.495221e6

ReadPosRankSum
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SIO_000300: 1.97e-1

MQRankSum
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MQ
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SIO_000300: 5.967e1

InbreedingCoeff
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SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

FS
type: SiteQuality
SIO_000300: 5.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 900
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66532
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South Asian
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allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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QD
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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GenotypeDepth
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variant carriers: 1

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

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

Other
type: Population
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allele frequency: 1.111111111111111e-3
allele num: 900
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 3
allele frequency: 4.674353381115612e-4
allele num: 6418
num of homozygotes: 0

South Asian
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allele num: 16488
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
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European (Non-Finnish)
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allele count: 15
allele frequency: 2.254689754689755e-4
allele num: 66528
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Other
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Latino
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num of homozygotes: 0

South Asian
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allele frequency: 7.885478587892757e-4
allele num: 16486
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66518
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InbreedingCoeff
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ClippingRankSum
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DP
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MQ
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BaseQRankSum
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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East Asian
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African
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European (Finnish)
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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DP
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FS
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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MQ
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FS
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QD
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MQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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African
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Latino
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European (Finnish)
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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DP
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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MQ
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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Other
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African
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European (Non-Finnish)
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FS
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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DP
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ClippingRankSum
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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African
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European (Non-Finnish)
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ReadPosRankSum
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FS
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ClippingRankSum
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MQ
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MQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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SIO_000300: 0.0e0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

FS
type: SiteQuality
SIO_000300: 2.264e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.979e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.689e1

DP
type: SiteQuality
SIO_000300: 1.476312e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 5931
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

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

GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65938
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6194
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.110975311659741e-5
allele num: 16364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

QD
type: SiteQuality
SIO_000300: 1.247e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.62e-1

FS
type: SiteQuality
SIO_000300: 4.043e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.016e0

DP
type: SiteQuality
SIO_000300: 1.470396e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 460
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 234
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GenotypeQuality
all individuals: 788
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516806212838248e-5
allele num: 65928
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
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: 10238
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.904e1

DP
type: SiteQuality
SIO_000300: 1.469821e6

InbreedingCoeff
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SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

QD
type: SiteQuality
SIO_000300: 1.087e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.321e0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 45299
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 698
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 639
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 258
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 665
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variant carriers: 0

GenotypeQuality
all individuals: 1458
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6114
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16234
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.762705923589205e-5
allele num: 11412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

QD
type: SiteQuality
SIO_000300: 8.24e0

DP
type: SiteQuality
SIO_000300: 1.453903e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.287e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.48e-1

FS
type: SiteQuality
SIO_000300: 3.212e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

GenotypeDepth
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 874
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 201
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GenotypeQuality
all individuals: 622
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
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: 16110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65368
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.798169980644026e-5
allele num: 11366
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: 7.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.341e0

VQSLOD
type: SiteQuality
SIO_000300: 6.59e-1

BaseQRankSum
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QD
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SIO_000300: 1.472e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.438477e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 198
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530549773478634e-5
allele num: 65336
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6052
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.640845070422535e-4
allele num: 11360
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.397e0

FS
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ReadPosRankSum
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MQRankSum
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DP
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.948e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10046
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.542305438168975e-5
allele num: 64838
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 4.92e0

DP
type: SiteQuality
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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SIO_000300: 7.04e-1

BaseQRankSum
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SIO_000300: -7.18e-1

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

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 5.043373007867661e-4
allele num: 9914
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.563966218329684e-4
allele num: 63940
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 9.433072351664937e-5
allele num: 63606
num of homozygotes: 0

Latino
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Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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DP
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
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QD
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ReadPosRankSum
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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South Asian
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allele num: 15358
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MQ
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DP
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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South Asian
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Latino
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allele frequency: 9.117432530999271e-4
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num of homozygotes: 0

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

Other
type: Population
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num of homozygotes: 0

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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East Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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MQ
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Other
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South Asian
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Latino
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Other
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African
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South Asian
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Latino
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East Asian
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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FS
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VQSLOD
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 1.0991426687184e-4
allele num: 9098
num of homozygotes: 0

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

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

Latino
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East Asian
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MQ
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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ClippingRankSum
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MQRankSum
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FS
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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European (Non-Finnish)
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Other
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European (Finnish)
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East Asian
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQ
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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FS
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ReadPosRankSum
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InbreedingCoeff
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QD
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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South Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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QD
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FS
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BaseQRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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South Asian
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European (Finnish)
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European (Non-Finnish)
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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VQSLOD
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FS
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ReadPosRankSum
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

BaseQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQRankSum
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FS
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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DP
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QD
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MQRankSum
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

South Asian
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allele num: 16472
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.934e1

DP
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MQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.214034235765449e-4
allele num: 16474
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -8.64e-1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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QD
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GenotypeQuality
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variant carriers: 0

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

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

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

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

South Asian
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allele frequency: 2.424242424242424e-4
allele num: 16500
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
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VQSLOD
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DP
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MQRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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SIO_000300: 1.3e-2

GenotypeQuality
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variant carriers: 0

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

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

East Asian
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African
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South Asian
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Other
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MQ
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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Other
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DP
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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Latino
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Latino
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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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VQSLOD
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FS
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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MQ
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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Latino
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European (Non-Finnish)
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Other
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East Asian
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FS
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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QD
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MQ
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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QD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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MQ
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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South Asian
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East Asian
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Latino
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Other
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MQ
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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DP
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FS
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InbreedingCoeff
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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InbreedingCoeff
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FS
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MQ
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ReadPosRankSum
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VQSLOD
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QD
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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Latino
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South Asian
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MQ
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VQSLOD
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FS
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DP
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QD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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South Asian
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VQSLOD
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BaseQRankSum
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FS
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DP
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MQ
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InbreedingCoeff
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QD
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SIO_000300: 1.48e1

MQRankSum
type: SiteQuality
SIO_000300: -2.322e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.6e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

QD
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SIO_000300: 1.456e1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 5.88e-1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
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SIO_000300: -1.499e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.947e1

QD
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SIO_000300: 1.485e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.36e-1

DP
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SIO_000300: 1.678748e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
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SIO_000300: 4.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

DP
type: SiteQuality
SIO_000300: 1.678864e6

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

FS
type: SiteQuality
SIO_000300: 4.571e0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 1
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allele num: 11576
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.66e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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SIO_000300: -4.7e-2

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 5.98e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

African
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allele count: 0
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num of homozygotes: 0

East Asian
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allele count: 6
allele frequency: 6.934812760055479e-4
allele num: 8652
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
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FS
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QD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

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

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

South Asian
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allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

European (Finnish)
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Other
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Latino
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MQRankSum
type: SiteQuality
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MQ
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e-1

DP
type: SiteQuality
SIO_000300: 1.678597e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.49e0

MQRankSum
type: SiteQuality
SIO_000300: 6.29e-1

FS
type: SiteQuality
SIO_000300: 7.48e-1

QD
type: SiteQuality
SIO_000300: 1.546e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

GenotypeDepth
all individuals: 166
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1904
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1121
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9766
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44323
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.133e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 1.01e1

DP
type: SiteQuality
SIO_000300: 1.678633e6

QD
type: SiteQuality
SIO_000300: 1.507e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.044e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-1

GenotypeDepth
all individuals: 56
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44320
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2211
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9766
bin: 6.75e1
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: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0