15-101816781-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816781
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816781
    reference: chr 15
allele count: 1
allele frequency: 8.359945827551038e-6
allele num: 119618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.176G>A
  hgvsp: ENSP00000433541.1:p.Arg59Lys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.200G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.212G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.296G>A
  hgvsp: ENSP00000434842.1:p.Arg99Lys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.176G>A
  hgvsp: ENSP00000437381.1:p.Arg59Lys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.259G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.107G>A
  hgvsp: ENSP00000433803.1:p.Arg36Lys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.176G>A
  hgvsp: ENSP00000381282.3:p.Arg59Lys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.896G>A
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg59Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-101816782-TCAAGG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816782
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816777
    reference: chr 15
allele count: 1
allele frequency: 8.357709987463435e-6
allele num: 119650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.206_210delCCTTG
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.170_174delCCTTG
  hgvsp: ENSP00000381282.3:p.Ala57GlufsTer15
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.290_294delCCTTG
  hgvsp: ENSP00000434842.1:p.Ala97GlufsTer15
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.101_105delCCTTG
  hgvsp: ENSP00000433803.1:p.Ala34GlufsTer15
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.890_894delCCTTG
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.194_198delCCTTG
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.170_174delCCTTG
  hgvsp: ENSP00000433541.1:p.Ala57GlufsTer15
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.253_257delCCTTG
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.170_174delCCTTG
  hgvsp: ENSP00000437381.1:p.Ala57GlufsTer15
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3024
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7723
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala57GlufsTer15
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: TCAAGG
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

15-101816786-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816786
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816786
    reference: chr 15
allele count: 1
allele frequency: 8.348778573694668e-6
allele num: 119778
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.171C>T
  hgvsp: ENST00000398226.3:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.195C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.291C>T
  hgvsp: ENST00000528346.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.102C>T
  hgvsp: ENST00000531964.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.171C>T
  hgvsp: ENST00000526049.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.171C>T
  hgvsp: ENST00000537379.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.254C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.891C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.207C>T
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala57Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum

15-101816791-TTAGCCGGGCGGAAAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816791
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816776
    reference: chr 15
allele count: 1
allele frequency: 8.34278849362611e-6
allele num: 119864
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsp: ENSP00000381282.3:p.Leu51_Leu55del
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsp: ENSP00000433803.1:p.Leu28_Leu32del
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsp: ENSP00000437381.1:p.Leu51_Leu55del
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsp: ENSP00000434842.1:p.Leu91_Leu95del
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsp: ENSP00000433541.1:p.Leu51_Leu55del
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7752
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu51_Leu55del
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: TTAGCCGGGCGGAAAG
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

15-101816792-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816792
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816792
    reference: chr 15
allele count: 1
allele frequency: 8.34153584357952e-6
allele num: 119882
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.189A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.96A>G
  hgvsp: ENST00000531964.1:c.96A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.165A>G
  hgvsp: ENST00000526049.1:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.285A>G
  hgvsp: ENST00000528346.1:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.201A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.248A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.885A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.165A>G
  hgvsp: ENST00000398226.3:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.165A>G
  hgvsp: ENST00000537379.1:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3643
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu55Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-101816793-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816793
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816793
    reference: chr 15
allele count: 1
allele frequency: 8.338892595063375e-6
allele num: 119920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.284T>A
  hgvsp: ENSP00000434842.1:p.Leu95Gln
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.164T>A
  hgvsp: ENSP00000437381.1:p.Leu55Gln
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.247T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.884T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.200T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.95T>A
  hgvsp: ENSP00000433803.1:p.Leu32Gln
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.188T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.164T>A
  hgvsp: ENSP00000381282.3:p.Leu55Gln
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.164T>A
  hgvsp: ENSP00000433541.1:p.Leu55Gln
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu55Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

15-101816796-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816796
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816796
    reference: chr 15
allele count: 3
allele frequency: 2.500875306357225e-5
allele num: 119958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.185G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.281G>A
  hgvsp: ENSP00000434842.1:p.Arg94Gln
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.161G>A
  hgvsp: ENSP00000381282.3:p.Arg54Gln
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.161G>A
  hgvsp: ENSP00000437381.1:p.Arg54Gln
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.197G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.92G>A
  hgvsp: ENSP00000433803.1:p.Arg31Gln
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.881G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.161G>A
  hgvsp: ENSP00000433541.1:p.Arg54Gln
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.244G>A
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3644
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg54Gln
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

15-101816797-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816797
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816797
    reference: chr 15
allele count: 2
allele frequency: 1.666722224074136e-5
allele num: 119996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.91C>T
  hgvsp: ENSP00000433803.1:p.Arg31Trp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.160C>T
  hgvsp: ENSP00000433541.1:p.Arg54Trp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.243C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.880C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.196C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.160C>T
  hgvsp: ENSP00000437381.1:p.Arg54Trp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.280C>T
  hgvsp: ENSP00000434842.1:p.Arg94Trp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.184C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.160C>T
  hgvsp: ENSP00000381282.3:p.Arg54Trp
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2897
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2317
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg54Trp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD

15-101816797-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816797
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816797
    reference: chr 15
allele count: 16
allele frequency: 1.333377779259309e-4
allele num: 119996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.184C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.160C>G
  hgvsp: ENSP00000433541.1:p.Arg54Gly
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.280C>G
  hgvsp: ENSP00000434842.1:p.Arg94Gly
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.243C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.880C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.196C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.160C>G
  hgvsp: ENSP00000381282.3:p.Arg54Gly
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.160C>G
  hgvsp: ENSP00000437381.1:p.Arg54Gly
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.91C>G
  hgvsp: ENSP00000433803.1:p.Arg31Gly
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3041
  bin: 9.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg54Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

15-101816802-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816802
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816802
    reference: chr 15
allele count: 1
allele frequency: 8.329723786359244e-6
allele num: 120052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.275C>G
  hgvsp: ENSP00000434842.1:p.Ser92Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.179C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.155C>G
  hgvsp: ENSP00000433541.1:p.Ser52Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.155C>G
  hgvsp: ENSP00000437381.1:p.Ser52Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.875C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.86C>G
  hgvsp: ENSP00000433803.1:p.Ser29Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.155C>G
  hgvsp: ENSP00000381282.3:p.Ser52Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.191C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.238C>G
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser52Cys
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

15-101816804-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816804
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816804
    reference: chr 15
allele count: 1
allele frequency: 8.327088017320342e-6
allele num: 120090
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.153T>C
  hgvsp: ENST00000398226.3:c.153T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.189T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.177T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.273T>C
  hgvsp: ENST00000528346.1:c.273T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.873T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.236T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.153T>C
  hgvsp: ENST00000526049.1:c.153T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.153T>C
  hgvsp: ENST00000537379.1:c.153T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.84T>C
  hgvsp: ENST00000531964.1:c.84T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37871
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu51Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

15-101816808-TTCTGAAAGAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816808
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816798
    reference: chr 15
allele count: 1
allele frequency: 8.323206765102459e-6
allele num: 120146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsp: ENSP00000433541.1:p.Val47SerfsTer6
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsp: ENSP00000381282.3:p.Val47SerfsTer6
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.70_79delGTCTTTCAGA
  hgvsp: ENSP00000433803.1:p.Val24SerfsTer6
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsp: ENSP00000434842.1:p.Val87SerfsTer6
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsp: ENSP00000437381.1:p.Val47SerfsTer6
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35761
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7801
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3031
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val47SerfsTer6
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: TTCTGAAAGAC
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

15-101816809-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816809
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816809
    reference: chr 15
allele count: 2
allele frequency: 1.66461364317342e-5
allele num: 120148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.148A>G
  hgvsp: ENSP00000437381.1:p.Lys50Glu
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.79A>G
  hgvsp: ENSP00000433803.1:p.Lys27Glu
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.268A>G
  hgvsp: ENSP00000434842.1:p.Lys90Glu
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.868A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.172A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.148A>G
  hgvsp: ENSP00000381282.3:p.Lys50Glu
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.148A>G
  hgvsp: ENSP00000433541.1:p.Lys50Glu
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.184A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.231A>G
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7802
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys50Glu
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

15-101816811-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816811
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816811
    reference: chr 15
allele count: 3
allele frequency: 2.496546444085682e-5
allele num: 120166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.866A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.146A>G
  hgvsp: ENSP00000433541.1:p.Gln49Arg
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.170A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.77A>G
  hgvsp: ENSP00000433803.1:p.Gln26Arg
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.182A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.146A>G
  hgvsp: ENSP00000381282.3:p.Gln49Arg
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.146A>G
  hgvsp: ENSP00000437381.1:p.Gln49Arg
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.266A>G
  hgvsp: ENSP00000434842.1:p.Gln89Arg
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.229A>G
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln49Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

15-101816818-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816818
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816818
    reference: chr 15
allele count: 1
allele frequency: 8.318637074501714e-6
allele num: 120212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.70G>A
  hgvsp: ENSP00000433803.1:p.Val24Ile
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.139G>A
  hgvsp: ENSP00000437381.1:p.Val47Ile
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.139G>A
  hgvsp: ENSP00000433541.1:p.Val47Ile
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.139G>A
  hgvsp: ENSP00000381282.3:p.Val47Ile
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.259G>A
  hgvsp: ENSP00000434842.1:p.Val87Ile
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.222G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.859G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.163G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.175G>A
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3656
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val47Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

15-101816820-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816820
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816820
    reference: chr 15
allele count: 1
allele frequency: 8.318360284820657e-6
allele num: 120216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.68T>A
  hgvsp: ENSP00000433803.1:p.Val23Glu
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.137T>A
  hgvsp: ENSP00000381282.3:p.Val46Glu
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.857T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.161T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.257T>A
  hgvsp: ENSP00000434842.1:p.Val86Glu
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.137T>A
  hgvsp: ENSP00000437381.1:p.Val46Glu
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.173T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.220T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.137T>A
  hgvsp: ENSP00000433541.1:p.Val46Glu
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val46Glu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

15-101816822-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816822
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816822
    reference: chr 15
allele count: 2
allele frequency: 1.663367654152597e-5
allele num: 120238
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.135C>T
  hgvsp: ENST00000398226.3:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.855C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.135C>T
  hgvsp: ENST00000537379.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.171C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.159C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.218C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.255C>T
  hgvsp: ENST00000528346.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.66C>T
  hgvsp: ENST00000531964.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.135C>T
  hgvsp: ENST00000526049.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38032
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Tyr45Tyr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

15-101816822-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816822
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816822
    reference: chr 15
allele count: 1
allele frequency: 8.316838270762986e-6
allele num: 120238
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.171C>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.855C>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.66C>A
  hgvsp: ENSP00000433803.1:p.Tyr22Ter
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.218C>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.255C>A
  hgvsp: ENSP00000434842.1:p.Tyr85Ter
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.135C>A
  hgvsp: ENSP00000437381.1:p.Tyr45Ter
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.135C>A
  hgvsp: ENSP00000381282.3:p.Tyr45Ter
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.135C>A
  hgvsp: ENSP00000433541.1:p.Tyr45Ter
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.159C>A
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3654
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr45Ter
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

15-101816823-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816823
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816823
    reference: chr 15
allele count: 1
allele frequency: 8.317114959162966e-6
allele num: 120234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.65A>G
  hgvsp: ENSP00000433803.1:p.Tyr22Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.134A>G
  hgvsp: ENSP00000381282.3:p.Tyr45Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.134A>G
  hgvsp: ENSP00000437381.1:p.Tyr45Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.134A>G
  hgvsp: ENSP00000433541.1:p.Tyr45Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.217A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.254A>G
  hgvsp: ENSP00000434842.1:p.Tyr85Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.854A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.170A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.158A>G
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3653
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr45Cys
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

15-101816824-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816824
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816824
    reference: chr 15
allele count: 2
allele frequency: 1.663229326059477e-5
allele num: 120248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.216T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.853T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.157T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.253T>C
  hgvsp: ENSP00000434842.1:p.Tyr85His
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.133T>C
  hgvsp: ENSP00000433541.1:p.Tyr45His
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.169T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.133T>C
  hgvsp: ENSP00000437381.1:p.Tyr45His
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.133T>C
  hgvsp: ENSP00000381282.3:p.Tyr45His
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.64T>C
  hgvsp: ENSP00000433803.1:p.Tyr22His
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2329
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr45His
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-101816825-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816825
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816825
    reference: chr 15
allele count: 1
allele frequency: 8.315178526882972e-6
allele num: 120262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.132C>T
  hgvsp: ENST00000526049.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.852C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.168C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.156C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.132C>T
  hgvsp: ENST00000537379.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.63C>T
  hgvsp: ENST00000531964.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.215C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.132C>T
  hgvsp: ENST00000398226.3:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.252C>T
  hgvsp: ENST00000528346.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35761
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7801
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu44Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum

15-101816827-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816827
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816827
    reference: chr 15
allele count: 30
allele frequency: 2.494595044071179e-4
allele num: 120260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.166C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.61C>G
  hgvsp: ENSP00000433803.1:p.Leu21Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.130C>G
  hgvsp: ENSP00000381282.3:p.Leu44Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.850C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.130C>G
  hgvsp: ENSP00000433541.1:p.Leu44Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.154C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.213C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.250C>G
  hgvsp: ENSP00000434842.1:p.Leu84Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.130C>G
  hgvsp: ENSP00000437381.1:p.Leu44Val
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu44Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

15-101816829-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816829
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816829
    reference: chr 15
allele count: 1
allele frequency: 8.314625426124552e-6
allele num: 120270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.848T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.128T>A
  hgvsp: ENSP00000437381.1:p.Leu43His
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.128T>A
  hgvsp: ENSP00000433541.1:p.Leu43His
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.248T>A
  hgvsp: ENSP00000434842.1:p.Leu83His
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.59T>A
  hgvsp: ENSP00000433803.1:p.Leu20His
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.152T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.128T>A
  hgvsp: ENSP00000381282.3:p.Leu43His
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.211T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.164T>A
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2909
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3659
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu43His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-101816848-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816848
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816848
    reference: chr 15
allele count: 62
allele frequency: 5.15695440254188e-4
allele num: 120226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.192A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.109A>G
  hgvsp: ENSP00000437381.1:p.Ile37Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.109A>G
  hgvsp: ENSP00000381282.3:p.Ile37Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.829A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.133A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.40A>G
  hgvsp: ENSP00000433803.1:p.Ile14Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.229A>G
  hgvsp: ENSP00000434842.1:p.Ile77Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.109A>G
  hgvsp: ENSP00000433541.1:p.Ile37Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.145A>G
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35479
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14541
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile37Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ

15-101816849-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816849
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816849
    reference: chr 15
allele count: 1
allele frequency: 8.317945134833891e-6
allele num: 120222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.108C>T
  hgvsp: ENST00000537379.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.108C>T
  hgvsp: ENST00000526049.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.828C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.191C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.108C>T
  hgvsp: ENST00000398226.3:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.144C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.39C>T
  hgvsp: ENST00000531964.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.132C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.228C>T
  hgvsp: ENST00000528346.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7757
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr36Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

15-101816850-T-TACC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816850
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816853
    reference: chr 15
allele count: 8
allele frequency: 6.656349325212588e-5
allele num: 120186
alternate allele: TACC
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.104_106dupGGT
  hgvsp: ENSP00000437381.1:p.Trp35dup
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.224_226dupGGT
  hgvsp: ENSP00000434842.1:p.Trp75dup
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.35_37dupGGT
  hgvsp: ENSP00000433803.1:p.Trp12dup
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.140_142dupGGT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.128_130dupGGT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.104_106dupGGT
  hgvsp: ENSP00000433541.1:p.Trp35dup
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.104_106dupGGT
  hgvsp: ENSP00000381282.3:p.Trp35dup
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.824_826dupGGT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.187_189dupGGT
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Trp35dup
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/15-101816851-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816851
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816851
    reference: chr 15
allele count: 419
allele frequency: 3.572890374513951e-3
allele num: 117272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.189T>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.106T>G
  hgvsp: ENSP00000381282.3:p.Tyr36Asp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.106T>G
  hgvsp: ENSP00000437381.1:p.Tyr36Asp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.130T>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.226T>G
  hgvsp: ENSP00000434842.1:p.Tyr76Asp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.142T>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.37T>G
  hgvsp: ENSP00000433803.1:p.Tyr13Asp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.106T>G
  hgvsp: ENSP00000433541.1:p.Tyr36Asp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.826T>G
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 3.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 34575
  bin: 2.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13920
  bin: 2.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 3.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.25e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.5e0
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 3.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 9.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 8.75e1
  variant carriers: 8
hgvs: p.Tyr36Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

15-101816852-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816852
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816852
    reference: chr 15
allele count: 1
allele frequency: 8.314348903337379e-6
allele num: 120274
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.105G>C
  hgvsp: ENSP00000381282.3:p.Trp35Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.129G>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.825G>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.105G>C
  hgvsp: ENSP00000437381.1:p.Trp35Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.105G>C
  hgvsp: ENSP00000433541.1:p.Trp35Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.36G>C
  hgvsp: ENSP00000433803.1:p.Trp12Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.188G>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.225G>C
  hgvsp: ENSP00000434842.1:p.Trp75Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.141G>C
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6118
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7734
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3774
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Trp35Cys
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/15-101816856-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816856
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816856
    reference: chr 15
allele count: 1
allele frequency: 8.321682977165302e-6
allele num: 120168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.101G>T
  hgvsp: ENSP00000437381.1:p.Gly34Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.137G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.821G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.221G>T
  hgvsp: ENSP00000434842.1:p.Gly74Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.184G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.101G>T
  hgvsp: ENSP00000433541.1:p.Gly34Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.101G>T
  hgvsp: ENSP00000381282.3:p.Gly34Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.32G>T
  hgvsp: ENSP00000433803.1:p.Gly11Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.125G>T
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly34Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

15-101816858-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816858
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816858
    reference: chr 15
allele count: 1
allele frequency: 8.320990530712775e-6
allele num: 120178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.99T>C
  hgvsp: ENST00000526049.1:c.99T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.99T>C
  hgvsp: ENST00000398226.3:c.99T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.123T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.219T>C
  hgvsp: ENST00000528346.1:c.219T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.99T>C
  hgvsp: ENST00000537379.1:c.99T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.819T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.135T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.182T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.30T>C
  hgvsp: ENST00000531964.1:c.30T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2331
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr33Tyr
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: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

15-101816859-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816859
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816859
    reference: chr 15
allele count: 2
allele frequency: 1.664225802156837e-5
allele num: 120176
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.98A>G
  hgvsp: ENSP00000381282.3:p.Tyr33Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.98A>G
  hgvsp: ENSP00000433541.1:p.Tyr33Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.134A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.818A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.218A>G
  hgvsp: ENSP00000434842.1:p.Tyr73Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.29A>G
  hgvsp: ENSP00000433803.1:p.Tyr10Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.98A>G
  hgvsp: ENSP00000437381.1:p.Tyr33Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.122A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.181A>G
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37227
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr33Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-101816862-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816862
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816862
    reference: chr 15
allele count: 3
allele frequency: 2.49804319949373e-5
allele num: 120094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.815C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.95C>T
  hgvsp: ENSP00000433541.1:p.Thr32Ile
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.215C>T
  hgvsp: ENSP00000434842.1:p.Thr72Ile
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.26C>T
  hgvsp: ENSP00000433803.1:p.Thr9Ile
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.131C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.95C>T
  hgvsp: ENSP00000381282.3:p.Thr32Ile
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.119C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.95C>T
  hgvsp: ENSP00000437381.1:p.Thr32Ile
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.178C>T
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3579
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr32Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

15-101816863-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816863
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816863
    reference: chr 15
allele count: 7
allele frequency: 5.829155771696951e-5
allele num: 120086
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.814A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.25A>G
  hgvsp: ENSP00000433803.1:p.Thr9Ala
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.177A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.214A>G
  hgvsp: ENSP00000434842.1:p.Thr72Ala
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.94A>G
  hgvsp: ENSP00000381282.3:p.Thr32Ala
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.94A>G
  hgvsp: ENSP00000433541.1:p.Thr32Ala
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.94A>G
  hgvsp: ENSP00000437381.1:p.Thr32Ala
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.118A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.130A>G
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3578
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr32Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

15-101816864-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816864
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816864
    reference: chr 15
allele count: 1
allele frequency: 8.330278897737497e-6
allele num: 120044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.813C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.176C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.213C>T
  hgvsp: ENST00000528346.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.93C>T
  hgvsp: ENST00000526049.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.117C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.93C>T
  hgvsp: ENST00000398226.3:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.93C>T
  hgvsp: ENST00000537379.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.129C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.24C>T
  hgvsp: ENST00000531964.1:c.24C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37054
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala31Ala
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

15-101816868-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816868
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816868
    reference: chr 15
allele count: 4
allele frequency: 3.334889615153738e-5
allele num: 119944
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.89T>C
  hgvsp: ENSP00000433541.1:p.Leu30Pro
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.209T>C
  hgvsp: ENSP00000434842.1:p.Leu70Pro
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.125T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.20T>C
  hgvsp: ENSP00000433803.1:p.Leu7Pro
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.89T>C
  hgvsp: ENSP00000381282.3:p.Leu30Pro
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.113T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.89T>C
  hgvsp: ENSP00000437381.1:p.Leu30Pro
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.172T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.809T>C
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3780
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2814
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu30Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-101816874-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816874
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816874
    reference: chr 15
allele count: 1
allele frequency: 8.368060785593547e-6
allele num: 119502
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.107C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.83C>G
  hgvsp: ENSP00000433541.1:p.Ser28Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.83C>G
  hgvsp: ENSP00000381282.3:p.Ser28Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.166C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.203C>G
  hgvsp: ENSP00000434842.1:p.Ser68Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.83C>G
  hgvsp: ENSP00000437381.1:p.Ser28Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.14C>G
  hgvsp: ENSP00000433803.1:p.Ser5Cys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.803C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.119C>G
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3777
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 986
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser28Cys
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

15-101816877-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816877
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816877
    reference: chr 15
allele count: 10
allele frequency: 8.385041086701326e-5
allele num: 119260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.200G>A
  hgvsp: ENSP00000434842.1:p.Gly67Asp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.11G>A
  hgvsp: ENSP00000433803.1:p.Gly4Asp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.163G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.80G>A
  hgvsp: ENSP00000437381.1:p.Gly27Asp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.80G>A
  hgvsp: ENSP00000433541.1:p.Gly27Asp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.800G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.104G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.80G>A
  hgvsp: ENSP00000381282.3:p.Gly27Asp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.116G>A
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33677
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7550
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly27Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

15-101816882-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816882
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816882
    reference: chr 15
allele count: 1
allele frequency: 8.42133629764371e-6
allele num: 118746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-2A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-2A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-2A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-2A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-2A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.795A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-2A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-2A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-2A>G
  variant of: http://identifiers.org/hgnc/30396
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1942
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.75e1
  variant carriers: 0
hgvs: c.77-2A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

15-101816892-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816892
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816892
    reference: chr 15
allele count: 1
allele frequency: 8.488964346349745e-6
allele num: 117800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.785T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-12T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-12T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-12T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-12T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-12T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-12T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-12T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-12T>A
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3783
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3542
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-101816892-AAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816892
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816890
    reference: chr 15
allele count: 6
allele frequency: 5.093378607809847e-5
allele num: 117800
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-14_197-13delGT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-14_8-13delGT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-14_101-13delGT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.783_784delGT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-14_160-13delGT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-14_77-13delGT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-14_77-13delGT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-14_77-13delGT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-14_113-13delGT
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7388
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: AAC
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

15-101816896-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816896
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816897
    reference: chr 15
allele count: 3
allele frequency: 2.550196365120114e-5
allele num: 117638
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-17dupA
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-17dupA
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-17dupA
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-17dupA
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-17dupA
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-17dupA
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.780dupA
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-17dupA
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-17dupA
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33365
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

15-101816897-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816897
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816897
    reference: chr 15
allele count: 1
allele frequency: 8.506294658046955e-6
allele num: 117560
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-17A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.780A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-17A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-17A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-17A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-17A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-17A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-17A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-17A>G
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2314
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

15-101816905-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816905
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816905
    reference: chr 15
allele count: 2
allele frequency: 1.708729901064539e-5
allele num: 117046
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-25T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.772T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-25T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-25T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-25T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-25T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-25T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-25T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-25T>C
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3518
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2771
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32231
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

15-101816907-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816907
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816907
    reference: chr 15
allele count: 2
allele frequency: 1.714207350521119e-5
allele num: 116672
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-27T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.770T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-27T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-27T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-27T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-27T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-27T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-27T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-27T>C
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3518
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/15-101816910-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816910
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816910
    reference: chr 15
allele count: 1
allele frequency: 8.582659594555161e-6
allele num: 116514
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-30T>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-30T>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-30T>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-30T>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-30T>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.767T>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-30T>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-30T>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-30T>G
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3783
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

15-101816914-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816914
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816914
    reference: chr 15
allele count: 28
allele frequency: 2.411838682446983e-4
allele num: 116094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-34T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-34T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-34T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-34T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.763T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-34T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-34T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-34T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-34T>C
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5536
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3407
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 1
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

15-101816921-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816921
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816921
    reference: chr 15
allele count: 1
allele frequency: 8.695349726966019e-6
allele num: 115004
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-41A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-41A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.756A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-41A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-41A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-41A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-41A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-41A>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-41A>G
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3506
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

15-101816922-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816922
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816922
    reference: chr 15
allele count: 1
allele frequency: 8.700040020184093e-6
allele num: 114942
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.755T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-42T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-42T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-42T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-42T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-42T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-42T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-42T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-42T>C
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29063
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

15-101816926-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101816926
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101816926
    reference: chr 15
allele count: 1
allele frequency: 8.73774531219964e-6
allele num: 114446
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.77-46C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.101-46C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.113-46C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.8-46C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.197-46C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.77-46C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.751C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.160-46C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.77-46C>T
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29905
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3792
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 971
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28002
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7052
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

15-101817258-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817258
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817258
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.196+39C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+289C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+289C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+289C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+289C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+289C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.419C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+289C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+228C>T
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1739
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ

15-101817270-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817270
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817270
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 722
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+277G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+277G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.407G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+277G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+277G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+277G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+216G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.196+27G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+277G>A
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

15-101817281-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817281
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817281
    reference: chr 15
allele count: 1
allele frequency: 8.361204013377926e-4
allele num: 1196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+205G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+266G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+266G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.196+16G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+266G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+266G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+266G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.396G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+266G>A
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4021
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

15-101817289-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817289
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817289
    reference: chr 15
allele count: 1
allele frequency: 5.753739930955121e-4
allele num: 1738
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+258T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+258T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.196+8T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+258T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+197T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+258T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+258T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.388T>C
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+258T>C
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3414
  bin: 2.25e1
  variant carriers: 0
hgvs: c.196+8T>C
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

15-101817294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817294
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817294
    reference: chr 15
allele count: 2
allele frequency: 9.606147934678194e-4
allele num: 2082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+253G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+253G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.196+3G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+253G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+253G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+253G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+192G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.383G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+253G>A
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3434
  bin: 2.25e1
  variant carriers: 0
hgvs: c.196+3G>A
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/15-101817314-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817314
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817315
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 4480
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+232dupT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.178dupT
  hgvsp: ENSP00000434842.1:p.Cys60LeufsTer54
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+171dupT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+232dupT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.362dupT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+232dupT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+232dupT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+232dupT
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+232dupT
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2822
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2690
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys60LeufsTer54
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

15-101817330-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817330
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817330
    reference: chr 15
allele count: 19
allele frequency: 2.589967284623773e-3
allele num: 7336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+217T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+217T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+217T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.163T>A
  hgvsp: ENSP00000434842.1:p.Cys55Ser
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.347T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+156T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+217T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+217T>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+217T>A
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1670
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2447
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys55Ser
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/15-101817348-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817348
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817348
    reference: chr 15
allele count: 1
allele frequency: 1.061796559779146e-4
allele num: 9418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+199G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.329G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+199G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.145G>T
  hgvsp: ENSP00000434842.1:p.Ala49Ser
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+199G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+199G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+138G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+199G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+199G>T
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala49Ser
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

15-101817376-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817376
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817376
    reference: chr 15
allele count: 1
allele frequency: 9.556574923547401e-5
allele num: 10464
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+171C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+171C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.301C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+171C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+171C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+171C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+110C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+171C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.117C>G
  hgvsp: ENST00000528346.1:c.117C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2668
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly39Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

15-101817410-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817410
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817410
    reference: chr 15
allele count: 4
allele frequency: 3.78931413414172e-4
allele num: 10556
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+137A>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+137A>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.83A>T
  hgvsp: ENSP00000434842.1:p.Asp28Val
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+137A>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+137A>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.267A>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+137A>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+76A>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+137A>T
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4000
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp28Val
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

15-101817431-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817431
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817431
    reference: chr 15
allele count: 1
allele frequency: 9.59140610013428e-5
allele num: 10426
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+116C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+116C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+116C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+116C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+55C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.246C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.62C>T
  hgvsp: ENSP00000434842.1:p.Ser21Leu
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+116C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+116C>T
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser21Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/15-101817433-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817433
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817433
    reference: chr 15
allele count: 2
allele frequency: 1.925298421255295e-4
allele num: 10388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+114G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+114G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+114G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.60G>T
  hgvsp: ENST00000528346.1:c.60G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.244G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+114G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+114G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+114G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+53G>T
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4328
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg20Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

15-101817435-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817435
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817435
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 10348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.242C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+112C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+51C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+112C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.58C>T
  hgvsp: ENSP00000434842.1:p.Arg20Trp
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+112C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+112C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+112C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+112C>T
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7018
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6489
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg20Trp
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

15-101817438-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817438
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817438
    reference: chr 15
allele count: 19
allele frequency: 1.869710686872663e-3
allele num: 10162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.239G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+109G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+109G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+109G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+109G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.55G>A
  hgvsp: ENSP00000434842.1:p.Glu19Lys
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+109G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+109G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+48G>A
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7025
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 9.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu19Lys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/15-101817453-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817453
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817453
    reference: chr 15
allele count: 1
allele frequency: 1.033912324234905e-4
allele num: 9672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+94G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+94G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+94G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+94G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+94G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+33G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.224G>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.40G>T
  hgvsp: ENSP00000434842.1:p.Ala14Ser
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+94G>T
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9059
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3349
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8278
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ala14Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

15-101817464-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817464
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817464
    reference: chr 15
allele count: 1
allele frequency: 1.086484137331595e-4
allele num: 9204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+83C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.213C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+83C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.29C>T
  hgvsp: ENSP00000434842.1:p.Pro10Leu
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+83C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+83C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+83C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+83C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+22C>T
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10734
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2616
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro10Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

15-101817464-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817464
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817464
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 9204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+83C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.29C>G
  hgvsp: ENSP00000434842.1:p.Pro10Arg
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+83C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+83C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.213C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+22C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+83C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+83C>G
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+83C>G
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10734
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro10Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

15-101817465-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817465
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817465
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 9098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+82C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+82C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+82C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.212C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+82C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+21C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.28C>T
  hgvsp: ENSP00000434842.1:p.Pro10Ser
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+82C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+82C>T
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10680
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro10Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

15-101817472-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817472
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817472
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 8826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.205C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+75C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+75C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+75C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+75C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.21C>T
  hgvsp: ENST00000528346.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+75C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7+14C>T
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+75C>T
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11418
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10083
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala7Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

15-101817486-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817486
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817486
    reference: chr 15
allele count: 1
allele frequency: 1.204238921001927e-4
allele num: 8304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  hgvsc: ENST00000526043.1:n.191G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  hgvsc: ENST00000398226.3:c.76+61G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  hgvsc: ENST00000526049.1:c.76+61G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  hgvsc: ENST00000528346.1:c.7G>A
  hgvsp: ENSP00000434842.1:p.Gly3Ser
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  hgvsc: ENST00000531964.1:c.7G>A
  hgvsp: ENSP00000433803.1:p.Val3Met
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  hgvsc: ENST00000534014.1:n.112+61G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  hgvsc: ENST00000537379.1:c.76+61G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  hgvsc: ENST00000529968.1:n.159+61G>A
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  hgvsc: ENST00000527833.1:n.100+61G>A
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14689
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13372
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val3Met
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

15-101817490-CATGGCTGCGCGTCGCAAAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101817490
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101817471
    reference: chr 15
allele count: 1
allele frequency: 1.235177865612648e-4
allele num: 8096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433541
  ensembl transcript: ENST00000526049
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000527833
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000381282
  ensembl transcript: ENST00000398226
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000437381
  ensembl transcript: ENST00000537379
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000529968
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000526043
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000433803
  ensembl transcript: ENST00000531964
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131871
  ensembl transcript: ENST00000534014
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131871
  ensembl protein: ENSP00000434842
  ensembl transcript: ENST00000528346
  gene symbol: VIMP
  variant of: http://identifiers.org/hgnc/30396
canonical: false
consequence: coding sequence
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: CATGGCTGCGCGTCGCAAAA

GenotypeQuality
all individuals: 7715
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 993
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2887
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3023
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37266
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16258
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66010
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.030502885408079e-4
allele num: 9704
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.533703e6

VQSLOD
type: SiteQuality
SIO_000300: -3.022e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 4.42e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

MQ
type: SiteQuality
SIO_000300: 5.727e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.384e0

QD
type: SiteQuality
SIO_000300: 1.672e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.243e0

GenotypeQuality
all individuals: 1048
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37299
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514417252241338e-5
allele num: 66032
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.48e1

MQRankSum
type: SiteQuality
SIO_000300: -4.052e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.222e0

DP
type: SiteQuality
SIO_000300: 1.534224e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.029e0

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 7.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.89e-1

GenotypeQuality
all individuals: 994
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7740
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variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3635
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2886
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512996641147457e-5
allele num: 66094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.955e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e-1

QD
type: SiteQuality
SIO_000300: 1.04e1

MQRankSum
type: SiteQuality
SIO_000300: 7.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.536616e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.061e0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37620
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3645
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 518
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variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 997
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447535e-5
allele num: 66140
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.136e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.43e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.167e0

MQ
type: SiteQuality
SIO_000300: 5.5e1

FS
type: SiteQuality
SIO_000300: 2.386e0

MQRankSum
type: SiteQuality
SIO_000300: -4.517e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

QD
type: SiteQuality
SIO_000300: 1.82e0

DP
type: SiteQuality
SIO_000300: 1.53833e6

VQSLOD
type: SiteQuality
SIO_000300: -4.803e-1

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 7752
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 99
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 997
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variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511807214344027e-5
allele num: 66146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: -4.556e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

QD
type: SiteQuality
SIO_000300: 1.069e1

DP
type: SiteQuality
SIO_000300: 1.538666e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7755
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3028
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 3643
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 37657
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2893
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.11545988258317e-5
allele num: 16352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66170
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 2.746e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 1.387e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.4e-1

DP
type: SiteQuality
SIO_000300: 1.538917e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.161e0

GenotypeQuality
all individuals: 37718
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3031
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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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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7760
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.027749229188078e-4
allele num: 9730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.221896383186706e-4
allele num: 16368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

FS
type: SiteQuality
SIO_000300: 2.055e0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

QD
type: SiteQuality
SIO_000300: 1.208e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

DP
type: SiteQuality
SIO_000300: 1.540182e6

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e-1

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
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variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1048
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variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3041
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 37742
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3645
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510482750286992e-5
allele num: 66204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

DP
type: SiteQuality
SIO_000300: 1.541523e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

FS
type: SiteQuality
SIO_000300: 1.374e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.401e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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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

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 3645
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.041931001147967e-5
allele num: 66204
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

East Asian
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allele count: 12
allele frequency: 1.39178844815588e-3
allele num: 8622
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.401e1

DP
type: SiteQuality
SIO_000300: 1.541523e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.84e-1

FS
type: SiteQuality
SIO_000300: 1.374e0

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.542296e6

MQRankSum
type: SiteQuality
SIO_000300: 5.85e-1

FS
type: SiteQuality
SIO_000300: 3.629e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

QD
type: SiteQuality
SIO_000300: 1.055e1

VQSLOD
type: SiteQuality
SIO_000300: 8.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

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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bin: 7.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509251713000694e-5
allele num: 66258
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.04e-1

QD
type: SiteQuality
SIO_000300: 1.102e1

DP
type: SiteQuality
SIO_000300: 1.542554e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508568670045861e-5
allele num: 66288
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.543386e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.76e-1

MQ
type: SiteQuality
SIO_000300: 5.521e1

QD
type: SiteQuality
SIO_000300: 2.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.698e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 1.784e0

MQRankSum
type: SiteQuality
SIO_000300: -4.863e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.017137340091721e-5
allele num: 66288
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.543449e6

VQSLOD
type: SiteQuality
SIO_000300: 1.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-1

FS
type: SiteQuality
SIO_000300: 4.043e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 1.622e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

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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bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508386629660915e-5
allele num: 66296
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9746
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

QD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.543828e6

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508022680661117e-5
allele num: 66312
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 9756
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East Asian
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allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Other
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allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.83e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.89e-1

BaseQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50793172085168e-5
allele num: 66316
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.929e1

FS
type: SiteQuality
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ClippingRankSum
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -6.33e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3037
bin: 9.75e1
variant carriers: 2

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66332
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.049600327936052e-4
allele num: 9758
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

FS
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

QD
type: SiteQuality
SIO_000300: 1.507e1

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 5.995e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

DP
type: SiteQuality
SIO_000300: 1.54455e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507567991316408e-5
allele num: 66332
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.507e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 1.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

DP
type: SiteQuality
SIO_000300: 1.54455e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQ
type: SiteQuality
SIO_000300: 5.995e1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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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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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bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507658907248824e-5
allele num: 66328
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.94e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.56e-1

FS
type: SiteQuality
SIO_000300: 2.971e0

QD
type: SiteQuality
SIO_000300: 1.188e1

DP
type: SiteQuality
SIO_000300: 1.544446e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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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bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014590618593995e-5
allele num: 66344
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.417e0

MQRankSum
type: SiteQuality
SIO_000300: -4.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.48e0

QD
type: SiteQuality
SIO_000300: 1.34e1

DP
type: SiteQuality
SIO_000300: 1.544725e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.079766536964981e-5
allele num: 16448
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66352
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.379e0

QD
type: SiteQuality
SIO_000300: 1.236e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.424e0

VQSLOD
type: SiteQuality
SIO_000300: 1.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 1.544615e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 9.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.67e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 9.75e1
variant carriers: 30

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66352
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 28
allele frequency: 2.868852459016393e-3
allele num: 9760
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.017e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

QD
type: SiteQuality
SIO_000300: 1.281e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

DP
type: SiteQuality
SIO_000300: 1.546079e6

FS
type: SiteQuality
SIO_000300: 5.52e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
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bin: 1.75e1
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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bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506977304921788e-5
allele num: 66358
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.02e-1

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.101e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.086427267194157e-5
allele num: 16430
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 58
allele frequency: 8.742839915586373e-4
allele num: 66340
num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.050440844781628e-4
allele num: 9754
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

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

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66338
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.087168249330411e-5
allele num: 16428
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.634e0

DP
type: SiteQuality
SIO_000300: 1.546614e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.652e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.048e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 9.66e0

GenotypeQuality
all individuals: 1050
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 37400
bin: 6.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2912
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7758
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.87032752952636e-4
allele num: 16426
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.547195e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.13e-1

QD
type: SiteQuality
SIO_000300: 1.897e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.087e0

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.821e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

GenotypeQuality
all individuals: 216
bin: 5.25e1
variant carriers: 18

GenotypeQuality
all individuals: 7430
bin: 6.75e1
variant carriers: 15

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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bin: 2.75e1
variant carriers: 16

GenotypeQuality
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bin: 1.75e1
variant carriers: 10

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 23

GenotypeQuality
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bin: 4.25e1
variant carriers: 21

GenotypeQuality
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bin: 3.25e1
variant carriers: 10

GenotypeQuality
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bin: 5.75e1
variant carriers: 16

GenotypeQuality
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bin: 6.25e1
variant carriers: 7

GenotypeQuality
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bin: 9.75e1
variant carriers: 206

GenotypeQuality
all individuals: 3449
bin: 7.75e1
variant carriers: 20

GenotypeQuality
all individuals: 2757
bin: 7.25e1
variant carriers: 19

European (Finnish)
type: Population
allele count: 71
allele frequency: 1.118815001575796e-2
allele num: 6346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 243
allele frequency: 3.773057574063723e-3
allele num: 64404
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 8.027522935779817e-3
allele num: 872
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.094588005850804e-5
allele num: 16408
num of homozygotes: 0

African
type: Population
allele count: 87
allele frequency: 9.497816593886464e-3
allele num: 9160
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.049195616693868e-3
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.692628650904033e-5
allele num: 11504
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.062e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e0

DP
type: SiteQuality
SIO_000300: 1.616006e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

FS
type: SiteQuality
SIO_000300: 3.13824e2

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-2

QD
type: SiteQuality
SIO_000300: 1.22e0

VQSLOD
type: SiteQuality
SIO_000300: -4.537e2

MQ
type: SiteQuality
SIO_000300: 5.92e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.786e0

GenotypeQuality
all individuals: 37286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
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variant carriers: 0

GenotypeQuality
all individuals: 48
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 993
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506387081224391e-5
allele num: 66384
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.585595e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.198e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.61e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.257e0

QD
type: SiteQuality
SIO_000300: 1.071e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 992
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variant carriers: 0

GenotypeQuality
all individuals: 107
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GenotypeQuality
all individuals: 15
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3776
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variant carriers: 1

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 7697
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variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507567991316408e-5
allele num: 66332
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e0

VQSLOD
type: SiteQuality
SIO_000300: -1.288e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

FS
type: SiteQuality
SIO_000300: 6.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.578e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

DP
type: SiteQuality
SIO_000300: 1.583838e6

QD
type: SiteQuality
SIO_000300: 8.24e0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 7693
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 476
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 4
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GenotypeQuality
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GenotypeQuality
all individuals: 49
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 1087
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GenotypeQuality
all individuals: 2826
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.01e-1

DP
type: SiteQuality
SIO_000300: 1.583713e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

QD
type: SiteQuality
SIO_000300: 9.42e0

GenotypeQuality
all individuals: 479
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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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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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507431637975218e-5
allele num: 66338
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

DP
type: SiteQuality
SIO_000300: 1.583895e6

QD
type: SiteQuality
SIO_000300: 1.318e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.6e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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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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variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66306
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.83665972817436e-4
allele num: 16334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.05e-1

DP
type: SiteQuality
SIO_000300: 1.582565e6

QD
type: SiteQuality
SIO_000300: 1.165e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.34e0

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
all individuals: 51
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GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 2822
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variant carriers: 0

GenotypeQuality
all individuals: 37127
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.122534230679972e-4
allele num: 8618
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.52e0

MQRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.312e-1

MQ
type: SiteQuality
SIO_000300: 5.897e1

DP
type: SiteQuality
SIO_000300: 1.583e6

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
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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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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508659706716553e-5
allele num: 66284
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.381e1

MQRankSum
type: SiteQuality
SIO_000300: -1.309e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.109e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e0

DP
type: SiteQuality
SIO_000300: 1.581967e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -7.731e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

FS
type: SiteQuality
SIO_000300: 1.543e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.386e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.643603436266543e-4
allele num: 8614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

FS
type: SiteQuality
SIO_000300: 1.188e0

DP
type: SiteQuality
SIO_000300: 1.580604e6

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.034e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.09e-1

GenotypeQuality
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bin: 7.25e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.028383381324558e-4
allele num: 9724
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66042
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
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: 888
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.572171e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.35e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.61e-1

FS
type: SiteQuality
SIO_000300: 2.636e0

MQ
type: SiteQuality
SIO_000300: 5.885e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

QD
type: SiteQuality
SIO_000300: 1.24e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 10
allele frequency: 6.281407035175879e-4
allele num: 15920
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65952
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.739e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.568256e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

QD
type: SiteQuality
SIO_000300: 1.125e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520542529574552e-5
allele num: 65766
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.762e0

VQSLOD
type: SiteQuality
SIO_000300: 8.169999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.145e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
SIO_000300: 4.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.556526e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65434
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15130
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.667013347200555e-5
allele num: 11538
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.54e1

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQ
type: SiteQuality
SIO_000300: 5.998e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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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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bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.169544884922212e-5
allele num: 65434
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15130
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

FS
type: SiteQuality
SIO_000300: 6.79e-1

DP
type: SiteQuality
SIO_000300: 1.532271e6

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQ
type: SiteQuality
SIO_000300: 5.998e1

VQSLOD
type: SiteQuality
SIO_000300: 3.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

QD
type: SiteQuality
SIO_000300: 1.54e1

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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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73370319001387e-4
allele num: 11536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.039068994181214e-4
allele num: 9624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65382
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.22e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.659999999999999e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.528351e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 630
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529847321237341e-5
allele num: 65366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14978
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.52649e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.63e0

QD
type: SiteQuality
SIO_000300: 1.763e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.068520052778545e-5
allele num: 65178
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.95e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

QD
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SIO_000300: 1.687e1

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: -2.095e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e0

DP
type: SiteQuality
SIO_000300: 1.511787e6

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
all individuals: 1084
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14456
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.086375964948884e-4
allele num: 9586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65066
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.504498e6

MQ
type: SiteQuality
SIO_000300: 5.891e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.14e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-1

QD
type: SiteQuality
SIO_000300: 1.542e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 170
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.538224888478696e-5
allele num: 65010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.109e0

QD
type: SiteQuality
SIO_000300: 4.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.501652e6

MQRankSum
type: SiteQuality
SIO_000300: -1.663e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.75e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 27

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Latino
type: Population
allele count: 28
allele frequency: 2.433936022253129e-3
allele num: 11504
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14134
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e-1

QD
type: SiteQuality
SIO_000300: 1.472e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.81e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 1.019e0

DP
type: SiteQuality
SIO_000300: 1.495877e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.87e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.645e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.485702e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.363e0

QD
type: SiteQuality
SIO_000300: 1.647e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550868486352357e-5
allele num: 64480
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.144e0

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.484846e6

QD
type: SiteQuality
SIO_000300: 1.62e1

GenotypeQuality
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bin: 3.25e1
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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bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64298
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13164
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.083e1

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

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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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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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 112
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: 14
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.6747e4

FS
type: SiteQuality
SIO_000300: 1.0976e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

Other
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MQ
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InbreedingCoeff
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QD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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VQSLOD
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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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Other
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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 360
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 8.0e-4
allele num: 1250
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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BaseQRankSum
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MQ
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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QD
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DP
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ReadPosRankSum
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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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Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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Latino
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South Asian
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European (Non-Finnish)
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allele frequency: 2.392344497607655e-3
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ReadPosRankSum
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QD
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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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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South Asian
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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: 0.0e0
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Other
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: NaN
allele num: 0
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East Asian
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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ClippingRankSum
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ReadPosRankSum
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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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Other
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Latino
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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MQRankSum
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MQ
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BaseQRankSum
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QD
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DP
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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FS
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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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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Latino
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QD
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BaseQRankSum
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MQ
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ClippingRankSum
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FS
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DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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African
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South Asian
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Other
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MQ
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQRankSum
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BaseQRankSum
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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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South Asian
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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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Other
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MQ
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MQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 2.5e-1
allele num: 4
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Latino
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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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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
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FS
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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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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variant carriers: 2

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 frequency: 0.0e0
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South Asian
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allele num: 7280
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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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Other
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MQRankSum
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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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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European (Finnish)
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ReadPosRankSum
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SIO_000300: 5.5e-1

MQRankSum
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FS
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MQ
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QD
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InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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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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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 frequency: 0.0e0
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African
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South Asian
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allele frequency: 2.663302495093917e-3
allele num: 7134
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East Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

QD
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
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num of homozygotes: 0

European (Finnish)
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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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African
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allele frequency: 0.0e0
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Other
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South Asian
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allele num: 6774
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ClippingRankSum
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InbreedingCoeff
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FS
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QD
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MQRankSum
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DP
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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African
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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DP
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Latino
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Other
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African
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South Asian
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East Asian
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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Other
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DP
type: SiteQuality
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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MQ
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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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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South Asian
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European (Non-Finnish)
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East Asian
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Other
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African
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European (Finnish)
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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QD
type: SiteQuality
SIO_000300: 8.82e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.715e0

DP
type: SiteQuality
SIO_000300: 1.12586e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
all individuals: 130
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1396
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 437
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1429
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2423
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.703577512776831e-4
allele num: 5870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e0

QD
type: SiteQuality
SIO_000300: 1.356e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.605e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.29e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.262e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.813e0

DP
type: SiteQuality
SIO_000300: 1.13056e5

MQRankSum
type: SiteQuality
SIO_000300: -6.26e-1